Medtech Mindset Software Development Rightley Mcconnell

EPISODE 12 – Med Device Software: Agility and Quality with Rightley McConnell

In this episode,Rightley McConnell, VP of Operations at Precision Systems, Inc., covers how to maintain quality and speed when developing medical device software.

Rightley and Dan discuss:

  • Challenges to device software development for complex systems
  • Use of AGILE methodology and how to remain flexible in a regulated environment
  • Applicable standards, including 21 CFR 820, ISO 13485, IEC 62304, & ISO 14971
  • How quality can and should remain central at each development phase
  • And more

If you have any questions, please feel free to contact us or connect with Rightley.

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Episode Transcript

Dan Henrich:                       Hey, Rightley, thanks very much for coming on MedTech Mindset.

Rightley McConnell:              Absolutely. Thanks for having me.

Dan:                       It’s great to have you here and have PSI involved. Just so our listeners get to know you a little bit, can you quickly introduce yourself and PSI, and tell us about the different types of projects that you guys work on in MedTech.

Rightley:              Sure. Starting with the company, we’re Precision Systems Incorporated. We’ve been in business since 1979, and we really focused on mission-critical, safety-critical systems that cannot fail. So we’re writing code that goes inside devices that are in operating rooms, in vitro diagnostics. They could also be a life sustaining type three types of devices, infusion pumps in the like. We’ll do consultation requirements, design, the software development, unit testing, final V&V, and anywhere, pretty much along the line, also post-market. Once something gets out, if a customer needs some changes, we can help them with controlling that and updating the code, getting it back out to the field. So I’m the Vice President of Operations here. I have been for about four years now. And I’m a recovering engineer. I started here as a software engineer. It was just my second job out of school, and so I’ve been here about 14 years.

Dan:                       Great, great. And how about the different areas you touch within the product development process? So you mentioned the types of devices you work on, but what are the main roles that you play as you interact with clients?

Rightley:              A lot of the roles that we play at the very early stages of product conception could be helping with getting requirements for even the product, in place. And then also working through, software requirements on down you might say. So helping those customers with understanding how to roll product requirements into software requirements, how to make sure that they have all the right planning in place, how to make sure that the software is properly designed first, then implemented well. And it’s really full stack from there on down. And then just of course, making sure that they’re following all of the right regulatory procedures and have all the right SOPs in place, so that when they get through and they submit to a 510(k) for instance, to the FDA, that all the documentation is there.

Dan:                       Okay. And we’re going to delve into our theme here shortly, which is, how to ensure speed-to-market, operating in an agile environment while maintaining high quality standards throughout the software development process. But can you just talk broadly a little bit about the main challenges that that folks developing software for critical medical devices face throughout the process?

Rightley:              Sure. There’s two main paths that the challenges come down. You have the human, the soft challenges, and it usually deals with education and making sure that folks understand when they go down this path, that the regulatory, the design, the documentation, everything that goes around the process that goes around the actual product development can be as much or more than the product development itself. So a lot of the challenges stem from that, and understanding and planning far enough out to make sure that they have realistic timelines and or able to get the right resources, the right stakeholders involved early enough, so that they have a product development that goes smoothly, as part of the overall development that has to be done in the company. So that’s one. And then of course there are always technical challenges.

Rightley:              Software is sometimes nothing but technical challenges on its rougher days. So a lot of the types of challenges come down the line with interfacing known hardware to unknown hardware. Interfacing different devices within a product suite. Anytime you have two different components or devices talking to one another, there’s opportunity for challenge. So usually, code within a system can be self-contained, and controlled, and the development is, I want to say free of surprise, but it has a certain level predictability to it. As soon as you start interfacing different systems together, and some are off the shelf, and some are custom, and some you’re developing as part of the product, that’s where technical challenge usually comes in.

Dan:                       Talking about this, maintaining high levels of quality through the development process, what are the applicable standards that come to play in your day-to-day?

Rightley:              So for medical devices, everything is really dictated and flows down from the FDA. And that’s 21 CFR part 820. And that really talks about overall medical device development and quality management. From that, we have gotten our quality management system because we focus on software, is really based around a standard called IEC 62304, which is a software development life cycle standard that is for medical devices. And so 820 flows down in points two 62304, as an appropriate set of standards to use for development of software.

Rightley:              So our quality management system here at PSI is built around that, and that quality management system is also appropriate and we have been able to be certified to ISO 13485. So that’s the medical device manufacturing standard. We’re manufacturing code. So our part of the system is just the software, so we are able to be certified to 13845 because we follow good manufacturing practice, which is 62304. So there’s a bit of a web of standards, but it really all flows down from 21 CFR 820, and that points to all the different standards that are appropriate for different aspects of product development.

Dan:                       Sure. And there’s one other that you didn’t mention that I just want to highlight, because I think it’ll come up which is ISO 14971, having to do with risk management. Can you talk a little how that plays into your process?

Rightley:              Yeah. Thank you. So a 14971 as you mentioned, talks about risk management. And it’s a risk-based approach to doing software development. So 62304, and 14971 really play together. So it’s all about identifying and mitigating risk, early in the product development process so that you can flow that down into your software development process, and make sure that you’re focusing on designing, developing and testing the right parts of the system, and really making sure that you’re maintaining that very high level of quality without testing everything needlessly to the same level that you might need to test the very most critical parts of the system.

Rightley:              That also helps you mitigate technical risk as well. When you’re doing that failure modes, and effects, criticality analysis, FMECA, which is prescribed by 14971, you’re going to identify technical risks in addition to patient risks. They’re just going to come out as part of the process. You set those aside, really, you focus on 14971 on the patient risk, but there’s technical risks also need to be examined. So in mitigating those risks early on, as part of a phase zero and doing that initial investigation into what the technical risks are, really can pay dividends down the line, and it really helps maintain schedule and keep your development on track, with fewer surprises down the road.

Dan:                       So let’s turn to the turn to the meat of our discussion, which is how to ensure speed-to-market, maintain an agile process, and maintain high quality standards throughout the software development process. I know every company who’s doing this type of work is going to follow somewhat of a phased approach, whether it’s Archimedic, PSI, or other players in the industry. But can you just walk us through your software development process by phase, and talk about the different types of activities that take place there, and how you operate to maintain quality, and move quickly?

Rightley:              We look at it as six phases. So our phase zero is investigation. Phase one is planning. Phase two is requirements realization. Phase three is V&V. Four, regulatory and product launch, and then five is post-market surveillance. So those are the six main phases that we go through. Phase zero, and the way that we really apply, we look back at that FMECA right away, and we start looking at what things do we need to focus on, and what risks do we need to mitigate from a technical aspect and also from a patient-risk aspect. And phase zero, really, the main goals for us in the software development aspects, are to come out of phase zero with a good software requirements spec, a good architecture, and usually that’s expressed in an architectural design chart, and good product requirements. So those are the main three things from the software aspect that we try to get out of phase zero.

Rightley:              Those are what really sets you up for success later on down the road. Requirements, we here at PSI, and I think most anybody that gets into any product development, know that requirements are the source of everything. It’s either the source of your problems or the source of your success. Having good product requirements means you could flow down to good hardware requirements, good software requirements, and that means that all the different parts of the system are being developed in harmony. So that’s really the goal of phase zero, is to walk out of it with all the stakeholders, pretty much understanding what the system needs to do in order to fulfill its goal and help the patient.

Rightley:              So phase one is planning. Planning, planning, planning. So it’s all about making sure that you can turn those requirements from a software perspective, into designs you can lay out. Sprint schedules, this is where the AGILE approach starts to come in, and where you can really plan out, now that you know what the product is really going to be, you can lay out how long it’s going to take to get there, and how you’re going to develop it. So the main thing to understand about planning is if you don’t have a plan, you can’t change it. So having a plan and a work breakdown structure that’s based on the requirements that flows down into sprints, and usually we set them up on about a monthly basis. Different companies find different things more useful. It could be six weeks, it could be two months. It depends on what the development cycle of the rest of the product is. But we find that setting up the sprints on a monthly basis right there in that planning phase is what really allows us to be agile and keep things moving throughout development.

Rightley:              There are always going to be roadblocks. There’s always going to be something that’s going to require you to wait on developing a certain aspect of the system. That’s why having the sprint plan is so great, because you move something from sprint three back to sprint one, and vice versa, and keep the whole project moving, even if one particular part of it is not really allowing you to progress. That’s a lot of the difference between the traditional V model, Waterfall model of software development, and applying some added agile methodologies within and overall SDLC or software development life cycle methodology.

Rightley:              So phase one really, the biggest thing there is to make sure that you have a plan. Break down the work, lay out a sprint schedule, and know that it’s going to change. So during that phase, it’s also a really good idea to understand how changes are going to be managed, how problems are going to be reported. All the SOPs, and all the standards that really are around product development, that’s the point where you make sure that those are in place, and all the stakeholders understand and agree those.

Rightley:              Because that, sometimes may seem a little bit just doing boring paperwork, but you wouldn’t believe how many times sitting down and getting all the stakeholders, software guys, hardware guys’ management, marketing, they all think a little bit differently, as you might imagine. And so having everybody sit around and agree to a plan about who’s responsible for what at what points, how changes get managed, when there’s a design freeze, laying that out all up front really helps get everybody on the same team. And good planning and a good start like that in that phase one is critical for letting all the different teams go and do their work and then come back together and make sure that everything plays together well.

Dan:                       Right. So phase zero, maybe you would say the big deliverables of that, or the hardcore requirements … Maybe I should say detailed requirements both from a-

Rightley:              Product requirements, software requirements, hardware requirements, electronics, those parts should all be really worked out as part of that first investigative phase.

Dan:                       And your Phase One deliverables will be a laid out schedule of sprints that everyone agrees to adhere to. And there is a plan for change management in place. Is that correct?

Rightley:              Absolutely. You must plan to change. And that’s also when the mechanical guys, the electronics, everybody makes sure that their schedules mesh together. It doesn’t mean that everybody gets started, runs off and begins doing work immediately as soon as that phase is closed out. It just means that everybody’s plan is laid out about when things have to be done so that nobody ends up being left behind on the critical path, and then playing catch up.

Dan:                       Right, right. Okay. So let’s move into phase two where I think is where the rubber really starts to meet the road with software, and all the quality standards that come to play, right?

Rightley:              Right. So this is where, as you said, the rubber meets the road with software development. Phase two, design realization, is, in software coding and parlance, this is implementation for us. So this is where we start executing on those sprints. We open every sprint at the beginning of the four weeks, let’s say, we have goals set out for what we’re going to achieve during that time and make sure that the sprint deliverables that we’ve set up are possible, because that’s a great time to stop and evaluate and figure out if we’re waiting on a piece of electronics to get there before we can write a little bit of code, or if we’re waiting on the marketing group to give some answer about a certain thing before it can progress, that’s where we’re trying to make sure for that sprint for that group of work, we’ve got the things that we need in order to actually execute.

Rightley:              So for that, let’s say four weeks, we’re writing code. So if you’re more so in the software world, you may have heard something called Test-Driven Development. There are some aspects of that in there, where essentially you’re writing automated code along with the software so that you know, as you write functions or groups of functions, that they do the operation that they’re supposed to, and then when you write additional functions to interface with them, you’re not breaking them. So it’s really, really important that during that sprint, while writing the code, write the automated unit tests along with it. It really helps to ensure quality. It helps getting your speed to market, and it also allows you to make other changes in other sprints elsewhere, without fear of breaking the code you already wrote. So it really sets you up for success in being able to apply those agile tenants, but not have to worry too much about what you’ve already done previously.

Rightley:              So throughout the sprint, we’re developing and then towards the end of the sprint, there’ll be a cut off. So it could be somewhere, usually in like week three of the four week, or it could be a little bit later, that’s where we’ll do any sort of integration, like a little bit higher-level testing, to make sure that everything that we’ve developed over the sprint functions properly. The idea, and what we found that our clients love is that they want a sprint-deliverable at the end of month, that is functional to a point, and everything in their works, because they want to be able to show progress. And this is great for an internal teams and external teams like us, alike, being able, for software, which is a mushy, amorphous thing that a lot of people think is a little bit of black magic, being able to show deliverables on a regular basis and be able to report about what is done and what’s functioning, and be able to say, “Yes, this works”, gives everybody else in the rest of the team a nice warm fuzzy when they can see that progress from month to month.

Rightley:              So really aim that at the end of the sprint you’re getting something that is well tested and works to the prescribed level, and then really that’s where we iterate through the phases. Just same process, opening the sprint, doing the work, closing the sprint and on and on and on. And throughout that at the beginning of each sprint, like I said, we’re making sure that everything that we have is available to us, that we can execute the sprint, and it allows us to be agile, move things from sprint to sprint, and try and keep the overall workload as flat as you can, because as you establish a team, you want to keep that team working on the project, you don’t want to scale up and scale down. Being a bit more agile allows you to do that most optimally, and most efficiently, and keep the fastest way to market is to keep a nice level workflow. So that’s what the sprints and being able to reorganize them as you go allows you to do.

Dan:                       Let’s jump into phase three, which is I think where a lot of the requirements and documentation really come into play, of how to, how to ensure the speed-to-market while maintaining quality.

Rightley:              Right. So we talked a little bit about, in the previous phase, we’re doing automated unit testing, which is one kind of verification. But the vast majority of the V&V, verification validation goes on in phase three. So that’s where at the highest level you’re taking the requirements that you developed early on, along with the FMECA, and getting the-

Dan:                       Sorry. One second. Before we go on, just tell us briefly … You mentioned the FMECA at the beginning, but just real quickly run through what that is and how it comes to play.

Rightley:              Sure. So what that essentially is, you could think of it as almost as a table or a spreadsheet and it often is organized as such. And it’s a listing of every risk and harm that can happen to the patient. There are entire standards and podcasts that could probably be done about how to do an effective FMECA. But really what you’re concerned about is getting all of the patient risks listed out, then understanding what’s the likelihood of that risk happening? So is it a one in 10 chance, or one in a million chance? How likely is it to happen once something gets into the field is being used by the patient? And not to mention that other stakeholders as well, especially like in, perhaps in in vitro diagnostics, there could be handling of blood where you have to be concerned, not only about, could you get a wrong result for the patient, but there are operators who have to handle blood. So you need to be thinking about the other stakeholders that are involved in the process as well.

Rightley:              So what’s the likelihood of this harm happening to them? And then also, what’s the severity? And understanding if something happens and it’s a minor inconvenience, that’s something that you can test to a certain degree, and you have to understand, you may not want to spend a man-year of development, in testing something that might cause five minutes and then inconvenience to somebody every 100 operating hours of the system. But things that could happen perhaps very rarely, but are very serious, you need to spend some time mitigating.

Rightley:              So the whole idea is that once you understand the criticality and the effects and the likelihood of something happening is how do you move those risks and mitigate those risks? What actions do you take throughout the rest of the development process? And especially in phase three when you’re doing a verification validation, to understand that those risks have indeed been mitigated and you’re not going to hurt somebody when this thing gets into the market. So that’s the main goal in FMECA.

Dan:                       Great. Okay. So back to what you’re saying about bringing the requirements in the FMECA into play here at phase three, let’s jump back into that.

Rightley:              Sure. So a really, at the highest level, that the FDA generally prescribes three levels of testing for software. There’s unit testing, there’s integration testing, and then there’s system-level testing. Unit testing we talked about, and that’s at the lowest level. We prescribe automated unit testing that is executed, it’s built alongside the code. That happens in phase two. Then some integration testing, where this is where you’re basically integrating components of the system. It could be software to hardware, it could be multiple software components together, you’re checking that they inter-operate correctly. So you’re making sure that during that phase, the software all plays together nicely with the other components of the system and itself. That can be done in an automated fashion, perhaps. It can also be done in a manual fashion. It can be done at the sprint level, but usually it happens more so long in phase three at the V&V phase. And then of course, there’s system-level tests. And system-level verification is the one that I think, the vast majority of what people understand verification to be, that’s where that happens.

Rightley:              So that’s where you’re looping back, looking at the software requirements that you developed early on in the system. And you may have modified and updated a bit through the design realization, but making sure that the system hits all of those requirements. And that by nature of hitting those requirements, it’s fulfilling the product requirements, and fulfilling the intended use to the customer, to the patient. So that’s where the vast majority of V&V activities come into play. That’s writing and executing those step-by-step tests.

Rightley:              You can write a lot of your system-level verification very early in the process, in the planning stage, and it’s highly recommended to do that. But quite often you’ll have to update those as you go through design realization, and you get to that final place where you’re going to start doing dry runs of your system-level verification, and then doing the official run of your system-level verification on the software.

Rightley:              The FMECA really comes into play there because you need to make sure that you’re not only testing that mitigation that you came up with via the steps, but you’re also making sure that you’re focusing in the right areas of the system. You may write many test plans that are, let’s say for instance, I’m talking about an in vitro diagnostic device. Just theoretically, you’re looking for some type of cell in a blood sample for instance. That’s the whole purpose of the device. Just as a theoretical, for instance. Your FMECA and therefore your testing is going to dictate that you spend a lot of time verifying, and later on validating that the software indeed is able to find with high levels of specificity and sensitivity, the particular type of blood cell that you’re looking for. That’s very important, and a lot of your tests should be written around that of course, when you think.

Rightley:              But on the same hand, you need to verify that you can quickly and easily flow through all of the screens in the workflow without having any problems with clicking and navigating from screen to screen. So it could cause a little bit of confusion or if there were some problem where you couldn’t navigate from screen to screen, that can be a real inconvenience. Especially if it’s one of those things that it might happen one time out of 100. It’s an annoyance. But worst case scenario, you run the test again.

Dan:                       It’s not the same as having a false negative for HIV blood test or something like that.

Rightley:              Yeah. A false positive or worse, a false negative. Right?

Dan:                       Right.

Rightley:              So that’s where you need to focus in that V&V stage when you’re writing those verification and then later on for the overall product validation, where you’re really focusing on the items that are really high-criticality and likelihood to occur from the FMECA. There’s another good point to point out too, that the quality of your software requirements really dictate how much trouble you’re going to have when you get to this stage. I think of it as there are “four Cs” for a good software requirement. And these will be; complete, correct, concise and you need to be able to confirm it.

Rightley:              So complete, as in, each requirement in your software requirements needs to express a complete thought. It might mean that there is a button on the screen that does this. There is the ability to handle the intake of a patient sample. There are workflows that hit the patient data input, and the screen outputs. Those all might be different requirements, but each requirement should be a complete statement or thought. Just like we learned back in grammar school that each sentence should be a complete thought, so should each requirement.

Rightley:              It needs to be correct. That seems obvious, but it needs to be reviewed that it’s correct and it doesn’t conflict with other requirements that are in the document. You wouldn’t believe how many software requirements documents that we’ve looked at or that we’ve seen, where you can pick out two or three in the same section that all conflict with one another. It’ really helpful to get people that are not even necessarily deep into the software development process, to give those a look through and make sure that it makes sense to them. Good software requirements should make sense to pretty much anybody that reads them.

Rightley:              So they should be concise. One of the biggest places that we see software requirements problems are in big long narrative requirements, when it really should be broken up into maybe 10 or 12 different requirements, instead of a paragraph. Testing a paragraph in phase three with software, with concise followable steps that can be repeated, trying to test that the requirement has been met when it’s 15, 16 sentences long is really, really difficult. And it leaves a lot of openness to interpretation. So it’s really important that your requirements be concise.

Rightley:              And finally, they need to be confirmable. So having good requirements that are testable, that don’t say things like the system must run indefinitely. You can’t test assist them indefinitely. So how would you ever know if you met that requirement? It shall be easy to use. How is it easy to use? That needs to flow down into very specific requirements, because you can’t test, is the system easy to use? It’s great to have those goals of being easy to use and being 100% uptime, but you need to have a confined confirmable requirement that you can test. If you follow those four Cs at the beginning in phase zero, it makes phase three way easier. So that’s big tips for verification, validation software.

Dan:                       Great. Okay. So phase four where we get into the regulatory submission, maybe not a particularly time-consuming part of the process, but it’s where you find out if you have done phases zero through three correctly, right?

Rightley:              Yeah.

Dan:                       So tell us a little bit about how the standards come into play. And obviously, if this phase doesn’t go well, then your time-to-market is going to be set back considerably.

Rightley:              Considerably. Yeah. So this is where all the previous phases really pay off, where you find out what you didn’t do right, as you said. So most of the software team’s role as we found, when it comes to this, is helping to put together the submission for the 510(k). So that means going back through making sure that your traceability from requirements through design, through implementation, through test is all complete. Making sure that you have all the prescribed documentation. The FDA is great in that the regulations are out there. You can find what needs to be submitted for a 510(k), just by going to the FDA website. And they list off all the documents and everything from a software perspective that you need to have. Even list off the types of testing that we were talking about.

Rightley:              That stuff is all there and when you’re trying to put together the 510(k), that’s when you find out whether or not the software team did their part. So that’s where you can either find that we’re going to have a nice 90 day window, where the FDA is reviewing our submission, or we’re going to be sent back to the drawing board several times to, hopefully not recreate, but find in our documentation package, in the code, where we tested this, where we explain that, and how we did everything.

Dan:                       So let’s talk about…you get sent back to the drawing board, which from time to time may happen even with the best laid plans. Where does the AGILE methodology come into play, and how do you go about relaying out, getting a tourniquet on this time-suck, to ensure that you’re addressing those things as quickly as possible and that it’s going to go through the second time.

Rightley:              Sure. There’s nothing saying that you can’t apply these AGILE methodologies to the requirements and the documentation and the design phases as well. So it’s like setting up a new sprint. When something gets identified and you can’t just go back and point to in the document where that item is discussed, if you need to do additional mitigation, you need to do additional documentation, you need to have some additional processes set up or some SOPs put into place, that’s like another sprint in the AGILE methodology. So if you do it very much the same way. As I mentioned before, it’s all about taking the sprint inputs, figuring out, “Do we have everything that we need? Who are the stakeholders that we need to pull in? How do we get consensus around the work that needs to be executed?”

Rightley:              You plan that sprint’s work. And that could be documentation work, it could be design work, it could be development, it could be retesting or testing further something, making sure that a risk has been mitigated, and then you execute on the sprint. So you’re really following that same opening, working, closing the sprint methodology that you would during the whole development phase. So it’s all about planning your work, executing the work, and making sure that the work that you did is well tested and integrates well into the rest of the system. And it could be software, it could be documentation, it could be anything.

Dan:                       So phase five then is the post-market phase, right? During which time you’re required to conduct post-market surveillance for your device. Right? Monitor what type of adverse events might be occurring, analyze their severity. Talk to us a little bit about the software maintenance and monitoring and retirement phase.

Rightley:              So the planning for how this is handled is actually is back in phase one. So how you’re going to handle change control, how you’re going to handle a configuration management of the software, how you’re going to handle when something comes in from the field, evaluating and going back through, perhaps adding to the FMECA based on information you get from the field, and then flowing that back through the process. So again, I don’t mean to sound like a broken record, but you’re really going to, again, apply that methodology, that AGILE methodology again, of evaluating what the information that comes in from the software perspective. Do we have to then flowing back through the requirements? Does it mean we need to change a requirement? Do we need to test a requirement differently? How does this affect the requirements? How does this affect the design? Where, if anywhere, do we need to make a change in the code? How does all of this get tested? And then how do we rerelease this back out into the field?

Rightley:              So it starts back at that FMECA, and it flows back through the whole process, but you set it up like a sprint. So what are your inputs for the sprint? What’s the work you need to do and what’s the output? How do you close the sprint out? So it’s all about change control and having those SOPs and having those standards in place, before you ever get to that point. You don’t want to be scrambling to figure out how are we going to handle this customer complaint, and this adverse effect reported from the field, because you don’t have an SOP in place. A worst case scenario, somebody hears something like that or a complaint comes in, and it just gets dropped or it’s not handled, or the software is never looked at because there’s no SOP. There’s nothing in place for how to handle something like that.

Dan:                       So let’s talk a little bit about what MedTech Innovation teams ought to have in place when they approach a software development partner. We’re talking starting in phase zero here. What do you expect them to have in hand, besides the funding? What do you expect them to have in hand when they come to you and say, “Rightley, I need your team to develop this system for me”?

Rightley:              Sure. Well, there’s usually difference between what we would like to have and what we expect that they have when they come. But we tend to help and get involved with anything from product requirements on down. Ideally, somebody comes to us and we’ve seen this a lot with startups, especially with serial entrepreneurs, and non-first time founders. They’ve been through this before. They understand what the outputs of a good phase zero, or it might be called a phase one in what they’re used to. But with the outputs of that are, and they come to us with software requirements that follow the four Cs. Or maybe they just need a little bit of a review and some questions to answer and they’re tweaked and we’re good to go. That’s ideal. And we’ve had some great customers that are startups. And again, usually it’s maybe not the founder’s first startup, but they come to us with those requirements.

Rightley:              What we oftentimes will get, is a long form narrative set of product requirements, and usually an explanation that goes along with it, and a fair amount of data and science behind it that says, “Here’s the medical problem that we’re tackling.” We get a lot of that. So a very often we will help them in forming those long-form narrative type of product requirements that are based in science and medicine, and starting to flow those down into short, testable product requirements, and then software requirements and on down.

Dan:                       Let me ask you a question that I’m sure a lot of your clients face, a lot of our early stage company clients encounter it at Archimedic, an early struggle is assembling enough funding to hire a vendor like PSI, like Archimedic, to help them develop their product. And they want to make sure that they are in the best position they can be, during all that time when they’re raising funds to be ready to start. What should a team be doing to get ready to launch into this process, with a software vendor?

Rightley:              In preparation for being able to bring a software vendor on board, or even if they’re choosing to hire software folks and bring them in house and have them as FTEs, be prepared by having at least identified somebody that’s in the regulatory realm, that understands the regulation that’s around their device. And maybe they haven’t actually engaged them yet, but have them on tap and know that you’ve got somebody that understands what regulation, and how it is going to apply, and that of course will flow down into software. Because we understand software very, very well, inside and out, but we don’t always understand the overall medicine behind it, and how the risks of software can actually flow upward to patient risks, and how the FDA is going to look at those.

Rightley:              So that person is really, really important, whether they’re in house or somebody else, you need to identify them. Having a good understanding of the addressable market and the product requirements, what the product needs to do is often oftentimes overlooked. And they could be long-form narrative requirements. But have something that at least, your internal stakeholders all understand and agree, because I can’t tell you how many different times we’ve been into what was supposed to be a software kickoff meeting, and some of the very basics about system operation and what the device must do, are still being hashed out around the table. So having all the stakeholders internally agreeing about what market they’re addressing, how the product’s going to be developed, what the product’s going to do, very important.

Rightley:              And then also before coming and looking for software vendors, review those standards that we talked about. You don’t have to be an expert. You don’t have to know 62304 inside now. But it’s written in fairly plain English. And you don’t have to read and understand every aspect of it, but the standards are all out there. Evaluation copies can often be obtained of like 62304, and some of the paid standards, just for educational purposes. But reviewing the 21 CFR 820, reviewing 62304, or at least understanding the overall software development life cycle, and reviewing ISO 14971, and what goes into risk management are a huge leg up in the understanding what’s about to come, what’s going to be in this process and understanding the overall effort that’s going to have to be applied around not just the product development itself, but everything that goes around it.

Dan:                      So one thing that we haven’t talked about but I’m sure is on a lot of listeners minds, talking about ensuring quality through the software development process, is cybersecurity, right? More and more devices are Internet connected. And there’s risks of malicious or unintentional interference with software that may be critical to a patient’s health or data security. Talk a little bit about how does that tie into your quality processes.

Rightley:              Sure. So no matter when you’re listening to this, there’s always going to be a recent data breach that keeps this fresh in people’s minds. And we get this question all the time. And it could be a podcast or an episode all into itself-

Dan:                       And I think it will be.

Rightley:              But from a software perspective … And there are a lot of facet to data security, cybersecurity. It’s not just software. There are hardware aspects. There are a lot of different … There’s a lot of network and infrastructure aspects that go along with it. But where it really comes into a lot of the software development that we do is it’s … It’s good best practices really are your best protection. You can go way into the weeds and there’s a lot of things that can be done, and security that can be added on top of a system, or built around a system, or in the network infrastructure where the system is connected. But a lot of it is just best practices. And unfortunately, a lot of the things that we hear about of cybersecurity problems with devices in the field, is where best practices just weren’t followed.

Rightley:              So those are things like, again, I hate to harp on requirements, but understanding back even at their requirements phase, who needs what access to what data when? And how is it tracked, if any of that access is made, or if data is changed? And how is that data protected? So is it encrypted when it’s sitting on the chip inside a device, or on a server or in a hard drive in a PC? Is it encrypted when it’s being transmitted across the network? Even a local network, is it an encrypted then? Is the appropriate level of access and password protection, and changing of passwords and everything, is that all built into the software from the beginning? So really, those are all best practices that that should be followed throughout the requirements, the design, and then of course in implementation. And then of course when you get into V&V, test them. Make sure that you’re doing a bit of penetration testing, make sure that you’re doing a bit of that button pushing, and trying to find those unintended consequential effects which may allow somebody access into a system.

Rightley:              It’s really hard to test everything of course, but really following good practices and shrinking your attack vectors is your best insurance. You can never be 100% sure that you’re invulnerable. It just doesn’t happen. There’s always vulnerability. The main thing is to make sure the devices and the things that you’re working on, have the smallest attack vectors possible. And that’s really your best insurance. It all comes from just following good practices, good requirements, good design, and using good off the shelf technologies and components that are well supported by the industry, and they’re being tested and proven everyday in use.

Rightley:              You’re right. You’re trying to eliminate surprises. That’s the whole point. So the whole point of applying this AGILE methodology throughout, and while maintaining the quality around the requirements is to eliminate surprises. You’re trying to mitigate those risks as many as you can figure out upfront, and you’re trying to make sure that each sprint you deliver has increasing levels of functionality and that they’re really no surprises from the previous one. So that’s how you’re really ensuring the speed-to-market. You can only make development go so fast. But you can try and eliminate as many surprises as you can, and try and make sure that you’re getting to market when you think you are, even if it’s not as fast as you had initially hoped.

Dan:                       So the term AGILE comes up a lot. I think people throw it around very casually and I think it’s leaked out of software into other disciplines. And there’s AGILE everything. What do you mean when you say AGILE methodology and why is it so critical to integrate it into the development of a Med device software system?

Rightley:              Sure. I think AGILE has gotten somewhat of a bad name over the years in the software development community because I think quite often, AGILE, and as I’ve heard it put, is not spelled A-D H-O-C. It’s not just an ad hoc methodology that allows us to develop a ‘fly by the seat of their pants’ and figure out today what they’re going to develop today. That’s not what AGILE is or supposed to be. There are a lot of flavors of it. And there’s a lot of different ways you can practice it, but they all have a lot of similarity in that it still means getting all of the stakeholders together, getting them to agree on what’s being developed, but being flexible in the way that you develop it. And I think that’s what we’ve really tried to implement here at PSI.

Rightley:              I’ve heard somebody called it that it’s the [wagile 01:20:41] methodology, a little bit what we practice because Waterfall methodology, if you’ve heard of that in software development, and that comes from electronics actually. So you add the Waterfall with requirements and design, you put that together with a sprint-wise development during the implementation phase, and you have [wagile 01:20:58], I’ve heard it called. So the way that, I think, like I said, it just gets a bit of a bad rep. And I think that it can be applied in a lot of different disciplines effectively. You could speak more to electromechanical than me for sure. But it needs to be built and deployed within a framework of good stakeholder agreement, and requirements, and knowing how you’re going to test it on the backend to make sure that that thing that you developed agilely actually does what it’s supposed to do.

Dan:                       I think we’re nearing the end of the time you’ve promised me. So I really appreciate Rightley, taking the time to come on and talk with me. If it’s all right, we’ll put your contact information in the blog post when we post this episode, and folks can get in touch with you if they want to if they want to pick your brain a little bit more.

Rightley:              We’re always happy to help. Getting somebody off to start the right way, it benefits everyone. So we’re always happy to take a phone call and help someone out.

Dan:                       Great. Hey, well thanks very much Rightley.

Rightley:              Thanks for having me.

Dan:                       Take care.

Written by Daniel Henrich

Written by Daniel Henrich

Director of Marketing at Archimedic

MedTech Mindset Podcast: Data Flow with Seth Goldenberg

EPISODE 11 – Data Flow & Medtech Innovation

In this episode, Seth Goldenberg, VP of Vault Medical Device & Diagnostics at Veeva Systems, covers data flow throughout the product lifecycle and how advanced data management can speed devices along the path to market.

Seth and Dan discuss:

  • How data management and accessibility impact the product lifecycle
  • What the device industry can learn from pharma’s data practices
  • How EU MDR is changing the data landscape
  • When in a device company’s growth does a cloud system start to make sense?
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Episode Transcript

Dan:                       Hey, Seth. Thanks so much for joining us today. It’s nice to have you on MedTech Mindset.

Seth:                     Yeah, no, happy to be here and look forward to the conversation.

Dan:                       Great. I’ve just introduced you obviously to our listeners, or at least I will have when we air this podcast. Your career, it seems to me anyway, has followed a pretty interesting, though maybe unexpected, path. At least when we heard that you had had taken your current position at Veeva, we thought, “well that’s a little out of step with where we would have maybe expected you to go next.” But I’m sure you have a good reason for it. Let me just ask you, I think you studied biomedical engineering and then did a PhD in structural biology and pharmacology. You’ve worked as a regulatory chemist at the FDA and then were at NAMSA in both regulatory and product development roles. That’s quite a variety of experiences. Then that led you to your position now as a VP at an enterprise software provider. Can you explain to us how you followed that path and what led you to your current role?

Seth:                     No, those are good questions and yeah, while the positions and the companies have changed the way that I’ve looked at my career has really been around trying to solve some problems, right? So, early in my career is really these hard science problems around basic mechanism of actions, structure function at the molecular level, looking at the pharmacology of doing x-ray crystallography and building crystal structures of large protein complexes to dive into how our cells are working, or these core problems. Then from there I went into drug discovery in the same field.

Seth:                     It’s continuing that same problem set. How do we now use this information to develop new therapies? So as a senior scientist at a drug startup, I learned a lot about that, started to get exposed to regulatory questions, the regulatory challenges that are in front of any product or drug that wants to come to the marketplace, and started to get interested in the regulatory side. I spent the first 10 years of my, let’s say career, as a student and then as a scientist in the field. Then I started to look at regulatory problems. So to answer that, I figured I should go to the place that makes the regulations, right, and is there to protect and promote public health.

Seth:                     I took a position at the FDA, began to learn more about that, understand the regulatory side. From that space too, I also learned about some of the challenges from the regulatory side at a global scale and started a consulting company in China. Again, still answering these regulatory questions. So, while the positions changed, I look at it as science, then regulatory, and that’s how I went into NAMSA continuing to answer those regulatory questions. Local Regulatory, which is what my role was at NAMSA.

Seth:                     Once I got to know NAMSA a little bit more though, the breadth and depth of services that they had from quality regulatory consulting, clinical trials, lab testing, back compatibility testing, there seemed to be a gap in the marketplace for expertise that was linked not only to these individual silos, let’s call them, these individual functions, when and how to use these different functions in product life cycle.

Seth:                     From there, that’s where I started the product development group at NAMSA. That was kind of the shift from the regulatory part of my career into how do I use this science background, this regulatory background ,to improve how products are brought to market, product life cycle. That’s how I got to know Veeva at the time too. Veeva was the ETMF provider that NAMSA used and still uses. They were one of our first device customers that Veeva had. As I continued to understand all the challenges that a company has in bringing a product to market, one of them in my experiences there, was really around data, and how do we share this information across these different processes.

Seth:                     So the groups that I put together at NAMSA, these teams of regulatory experts, quality expert, product engineers, reimbursement consultants, clinical trial experts, physicians, bringing all those people together, it very quickly became a problem to share information across these groups. I would actually have two people who all they did was just makes sure everyone knew what everyone else was doing and the timelines were being met. It just seemed very inefficient.

Seth:                     When the opportunity came up to work at Veeva and work on that technology side of the product, to me, while it might seem from the outside a little bit like jumping around, to me it was still that core problem about product life cycle. How do we manage that processes? What are the technologies that we can bring to bear to improve it and really help companies run and manage their businesses better?

Seth:                     I’ve been at a bunch of different places, but when I look at my career, I would say it’s been answering three problems. First it was hard science, then it was kind of figuring out some regulatory problems, and now, for the last part of my career and until what I’m currently doing, it’s that product life cycle management, bringing products to market and ways to do that differently so companies can worry less about their infrastructure and have a lot of meetings to just keep people up to speed when they could really be using technology in different ways to drive their products into the marketplace and get products to patients faster.

Dan:                       Obviously you then have had quite a bit of experience both with drugs and devices or devices and diagnostics. Being that you’ve been inside the FDA, outside the FDA, in consulting and in the industry, what are the broad trends that you see across how devices and drugs are maybe regulated and how similar and different are those trends, in terms of the regulatory environment and what impact they may have on product life cycles?

Seth:                     The regulatory environment, at the end of the day it’s all about, safety and effectiveness, right? Those are the core questions of any global regulator. The challenges or differences start showing up really fast though between drugs and devices, and that product life cycle’s a key part of that. When you bring a drug to market, you’re bringing that drug to market seven to 10 years. You also are then going to have a series of exclusivity and that drug is not going to change. The drug is the drug. It might go from a syringe into an auto injector to improve compliance, do some of these changes, change the dosage, but usually that’s it.

Seth:                     Whereas the device life cycle, even if you do a PMA, let’s say, you might be innovating on that PMA pretty quickly. You might be making changes a year, two years from now through the supplement process. Or a 501(k), obviously it’s every two years you have a new product on the market. The regulatory environments to address those questions just needs to be different because the life cycle is so different.

Seth:                     Some of the trends though that I’m seeing, of course, also, taking the regulations a step farther, the the shift to value on the payment side and on the market access side, is ones where I think they’re starting to converge again. It used to be that devices were much more transactional in nature around the procedures, and drugs have started that value discussion, it’s kind of the world in which they lived a little bit more.

Seth:                     But with the Affordable Care Act, the devices started to come back in to that value discussion. I think that’s actually good for devices, because instead of when you look at how payers, especially in the US used to look at the reimbursement scheme, it’d be “Am I going to get paid back in three years?” And if it was going take them longer to get reimbursed for the cost of a device procedure, they might not have gone after it. Neuromodulation is a great example, where they might have preferred to just keep on paying for pain medication as opposed to paying more for a neurostimulator that can then reduce that pain, but it’s also a lot more expensive procedure. Some of those shifts that are happening now in the device world and drug world are kind of coming back together in that market access space.

Seth:                     It’s a similar story that you’re starting to see globally for that, and it’s one that does have an impact on regulations. “What are my claims going to be? What’s my strategy going to be? What clinical data do I need to show, not only to the regulators but to the payers to show the value that I have in my product?”

Seth:                     It’s an interesting time, right? Especially with all the device regulations that are going on. In Europe IBDs are coming next from the European side and MDR 2020. IBD are 2022. Then the FDA is even making all these changes. They just completely restructured the whole device side of the business to align more, excuse me, the whole device part of the FDA is now aligned with therapeutic areas from approval through oversight, and there’s talk of how do we change the 510(k) process.

Seth:                     So the dynamic nature of the device world I don’t think is going to go away. I think the drug world is a lot more stable right now from the regulatory side, than the device world is. It’s going to be important to keep abreast of all those regulatory changes and think about how those regulations impact your product life cycle and your business.

Dan:                       Sure. Do you see trends in sort of growing public scrutiny where big Pharma kind of used to be the bad guy and it seems like maybe now med device is getting a little bit of that scrutiny, as well. Do you do see that and what do you think is driving that?

Seth:                     Yeah, and I think a lot of that is driven around of some of the… Any spaces always going to have bad actors that can that come up, but at the same time there are changes that probably needed to be done to improve the safety of devices, especially around the ongoing monitoring and the ability to see these safety trends. A single company might say, “Okay, well only one out of a hundred of my products is having an issue and we can manage that and we report that.” But when all of a sudden in that same device class goes to the FDA and all that information is put together, that then might present a different picture of a particular type of product.

Seth:                     The way that the safety set up was before in Europe, especially with the all the different notified bodies, lack of centralized reporting, the way that the FDA’s reporting and disclosures and the pace of which that had to happen, was letting some of those trends slip through or go unnoticed. I don’t think anyone is in the device world, again in general, there’s always bad actors out there, was having products with issues on the market, but just the way that the safety, the trending and the reporting was set up, really wasn’t set up until you would… it would take a long time for these to be noticed. I think some of the trends that are going on now on the safety side, are so you can see these things right away. You’re going to have adverse events in Europe. Now everything has to go into Eudamed right away. Really fast timeline, and you can see these trends and it’s across the all of Europe, not just a single notified body.

Seth:                     So I think it’s the reason that they’re getting that attention is because some of these systems need to be changed the way the products were marketed… so many products being brought to market quickly, right? I mean, there’s 2000 510(k)’s every year, relative to 50 drug approvals. It’s a big difference in terms of volume, so they need different environments, and I think the regulatory agencies are making the changes and trying out these new models to ensure that they work.

Seth:                     And it’s important to ensure that these products are still being… you don’t want to limit access to a new product or a new therapy that can help someone. You need to make sure that whole ecosystem is in place that still allows innovation and still allows patient access, but still has safety in a way that patients are protected.

Dan:                       Is that why Veeva is turning its attention to the device world, because of the increased expectation that you will collect and manage and analyze your data as part of your product development life cycle?

Seth:                     Well, I think part of it is just where Veeva is as a company. Veeva’s only 12 years old. We’re still a startup in a lot of ways and focus really does pay off, so focusing on the Pharma business and really establishing themselves in that space was the right calls. They could learn the product, really get deep into an industry, and support it. Now I think the time for beginning to focus on devices made sense. There’s a lot of maturity that Veeva has in the Pharma world. We’re the leading eTMF provider now in the clinical space for example, still a lot more work to do, a lot more innovation to be done.

Seth:                     So I think that’s one. Right? Just where Veeva was as a company. In addition, the MDR changes that were going on has awoken a lot of device professionals and a lot of device companies in how they need to look at managing their business and bringing their products to market. For example, the pace of innovation at device companies was so high they really just focused on on that. If there’s a regulatory change, they’ll just hire more regulatory people to keep on doing things the same way. “I have this two year launch window, I can’t deal with a whole business transformation. I’m just going to keep doing what I’m doing already. That’s my focus.”

Seth:                     MDR has really, I think brought to light in particular, as well as other other changes, but MDR in particular has brought to light to a lot of companies that the old way of doing things doesn’t work and they need to think differently about how they’re bringing their products to market, how they’re managing the life cycle, how they run their business and what they’re doing with their data.

Dan:                       Can you maybe expound a little bit? I think you’ve kind of alluded to that one of the reasons you were excited by joining the Veeva team and by Veeva’s expansion into device world is because you see ways in which it can shorten the product development life cycle and really help spur innovation at device development companies. Can you expound on that a little bit for our audience who maybe have had fewer conversations in the past year- [crosstalk 00:15:08]

Seth:                     [crosstalk 00:15:08] That’s a good question.

Dan:                       [crosstalk 00:15:09] than Eric or I have?

Seth:                     I think that the first one or the easiest one is really understanding the visibility to what’s going on across your company and the ability to collaborate across these different historically silos. As I was explaining it when I was at NAMSA, a lot of where I started to get interested was how do we break down these traditional barriers of being quality, regulatory, clinical and market access.

Seth:                     You know and can understand in one room, you don’t need to run multiple clinical trials to address all these different stakeholders. How do I design one study so the patients can understand the benefits to them, the payers understand the value, the regulators understand the safety and efficacy? But to do that you need to have a lot of visibility in the collaboration across your organization and having a cloud based system that everyone can have access to anywhere in the world and see what they need to see at the right time. While it sounds simple, it is very complicated and is also extremely powerful for an organization.

Seth:                     It allows them to unify a lot of their processes across whether it’s in a specific therapeutic area. Device companies therapeutic areas have a lot of differences in how the product life cycle, so that might be the level at which unification makes sense. Or it might be at the corporate level or could be you know, ordinance or something in between and mix of the two. The other big piece, and this comes and talks to an MDR in particular is really about am I audit ready? What’s my audit trail for my whole business process, not only on regulated documents that I’m going to submit as part of my review for my device, but just how I’m running my business, my sales and marketing material, all those changes. How can I be audited at any time and show that value? You show that trail to an auditor, right? You’re seeing changes not only from the FDA, the now notify bodies are doing it, surprise inspections, just like the FDA used to or still does.

Seth:                     The requirements to really be audit ready at all times as opposed to kind of catching up right when an audit starts is, is hugely beneficial.

Seth:                     So again, these are some of just the key things that folks, that companies are starting to think about on the device world or all the reasons we’ve talked about that. Again, Veeva the really fits nicely into, it’s what we’re focused on. Even three years ago, I don’t think device companies were quite ready for this, or ready to look at their businesses like this, and were just more focused on the current paradigms. It’s a good time to be regulatory professionals, there’s not enough of them, so you can’t find them. There’s not enough regulatory folks, their salaries are going up, you’re a big company, you can’t hire enough regulatory people with all these changes going on, so you need to look a little bit differently and what we’re doing and you really just don’t. And at the end of the day, you don’t want innovation to suffer because your business process to seize or the technology you’re using aren’t up to the task.

Dan:                       Right. Okay. So let me ask you, we have folks from companies of all different sizes listen to this podcast. Traditionally I’ve thought of Veeva as kind of a solution for only for the big kids, but in the med tech world, a lot of innovation as you know, happens at startups, small, mid sized companies and with the goal of de-risking it to the point where one of the big players is going to purchase them,

Dan:                       Is it too small minded for those companies to be thinking, “well, we’re gonna worry about managing all this data in the cloud later.” Are there ways that smaller companies could benefit from Veeva or a cloud based way of managing their data?

Seth:                     It’s a great question. So Veeva is a multi tenant cloud provider, so what that means, the analogy I like to use it as you think of the Veeva skyscraper, right? It has the same building, it’s the same plumbing, right? It has this same roof, but every company has their own apartments that has their own data. But what that means for a small company is, whether you have, 20 users, 50 users or 50,000 users, like some of our customers do, you’re getting this same technology. It’s extremely powerful for small companies, and in a lot of ways there’s probably more, yup. There’s a lot of benefit for small companies. I don’t want necessarily say more than big. It’s just different. The benefit that they get is is they’re making their staff, if they can’t go out and hire 20 new regulatory people, if there’s a regulatory change.

Seth:                     They need to do what they can with the staff they have, manage their burn rate, make sure that they’re collaborating and [inaudible 00:19:52] their company because they really can’t make mistakes. These big companies can absorb, if something doesn’t quite hit a timeline, they can absorb some of that. A small company, a couple months might be all you have in cashflow.

Dan:                       Right, sure.

Seth:                     Looking at and thinking about data flow at a small company, definitely mid size companies, is something that I think everyone should be doing. How am I bringing my [inaudible 00:20:16] It really answers that core question, how am I bringing my product to market? How am I managing that life cycle? How am I sharing information with all the key people that need to do it? In addition, one of the other advantages too for small companies is they’re probably having a lot of external partners but this makes sure they control their data and it’s not sitting on one CROS here, a product development company here or regulatory consultant over there.

Seth:                     They know where all their data is at one time and although all the data and documents are still together in one place, it’s unified and they can still connect with all those different partners. Veeva is a big company. We worked a lot of big Pharma. We work with a lot of small medical device companies too. We have over 80 customers in the device world today.

Seth:                     A lot of them are not very big, they have 25 employees, 50 employees, they’re not all the Medtronics of the world. I don’t even know how many that have 70,000 employees around the world. It’s something that I think anyone should be thinking about no matter where they are in their path to market.

Dan:                       Okay. Okay.

Dan:                       When would you say is, while you just kinda said no matter where they are, when would you say is time to get serious about moving from a paper-based to an electronic or to a cloud based like quality system for instance-

Seth:                     Yeah, I think that- [crosstalk 00:21:40]

Dan:                       [crosstalk 00:21:40] who should be the first actors at a device startup or pre-revenue device company to be doing that?

Seth:                     Well it probably depends on the product and what the barriers are. For example, if you’re going to be building a pretty complex device essentially a lot of different suppliers need to manage that flow, those SOPs, a lot of different contract manufacturers, that might make a lot of sense, even if you don’t necessarily have to do clinical trials. If you’re a really innovative product, first in human, first in man, you’re expecting a lot of clinical data to be coming in, it’s usually using CROs around the world that clinical might be your first step. So it’s probably one of those two. It’s probably gonna be-

Dan:                       [crosstalk 00:22:30] situational, right?

Seth:                     It’s probably gonna a quality opportunity or an opportunity for a company to go in and even just document management, even before QMS, where am I just managing my documents?

Seth:                     It might just be a document management perspective, not even a full QMS functionality yet and/or a clinical opportunity. This is my first in human and maybe I can get through with my first 10 patients on paper with this small CRO, but now I know that I’m going to be going to Europe for this study, I’m going to be running this study in the US and [inaudible 00:23:04] I want to control my data, I want to know where it is, I want to be audit ready. Those are also things you might be looking to internalize over time, so you don’t want to have to go and figure out where is all this information and I’m pulling it back from a [inaudible 00:23:18] and I’m building out my own clinical staff. I would say it’s typically probably one of one of those two, depending on the situation.

Dan:                       Let me shift the conversation a little bit and ask you about something that I’ve seen you kind of be very active in talking about on Linkedin and other places, and that’s, I always struggle with this, real world evidence.

Dan:                       Are there ways in which managing your data in a cloud system can inform that initiative, if the industry moves in that direction? What is it that’s got you specifically talking about, I’m just going to call it RWE because I’ll stumble again, and what excites you about it and how does it kind of tie into what you do in there on a day to day?

Seth:                     Yeah, real world evidence is something that’s really interesting, because the regulatory changes are requiring a collection of a lot more clinical data by companies, for safety and/or for showing the value as part of your market access, can show payers the value that your product has in the real world.

Seth:                     But it’s easy to say, right, [inaudible 00:24:39] sometimes easy to say real world evidence, but the challenge of how do I collect this data in a way that’s auditable? How do I collect this data in a way that I can clean it up, share it with regulatory authorities, potentially expand my regulatory claims, which is, if you look at the FDA guidance on real world evidence, is one of the things that they talked about, becomes very problematic. Right?

Seth:                     It’s one of those things that’s great in theory, but in practice it becomes very complicated. It’s something that cloud systems in particular are just really good at collecting data from all these different sources, organizing it and then disseminating it back out to the folks that need it. It’s something that one, is something that right now is looked at as a little bit as a cost center in device companies a lot.

Seth:                     Right now I have to do more trials, I have to collect more data, but in reality also has a lot of value. Bringing this together and figuring out the solution to this, how do I take this something that is costing me money to do it, if it’s cost to the system. How do I collect that in a way to help me with my regulatory story, help me with my payments [inaudible 00:25:43] is one that a lot of companies need to think about. The answer isn’t out there yet.

Seth:                     I actually have a panel at the Med Tech conference this year on this topic with Owen Farris, who was one of the leaders of this guidance and is the Director of Clinical Trials at the FDA, MDIC, who’s a consortium on this, is also going to be on the panel as well as industry. We’ll be talking about some of this because it’s had a lot of discussion in the last couple of years. Companies are starting to do it, start to generate that data, but there’s still a lot of unanswered questions, and it’s a good problem. I like being part of the dialogue and trying and help figure this out and look into the details of what it really needs to be and what the solution should be for the industry.

Dan:                       Yeah, absolutely. Thanks for bringing that up. I meant to plug that session. If any of our listeners are going to be there in Boston at the AdvaMed MedTech conference, end of September, Seth will be there leading a session, and Archimedic will be there too, so come by and meet us. We’d love to talk to you there about this and other related things.

Dan:                       Seth, I may be the last thing standing between you and your weekend and time for your family, so I appreciate you spending the time here. Got one more question for you before I let you go.

Dan:                       Just about MDR and, and its impact. You’ve touched upon it a couple times here, but people are really struggling to prepare for MDR by these upcoming deadlines. I see a lot of chatter about it in LinkedIn groups and I hear some anxiety from people in the industry. How do you see it impacting Med tech innovators? And if we’re talking about a pre-revenue stage company who maybe thinks our beachhead is in the US and Europe is the next step, what do they need to be thinking about when it comes to MDR?

Seth:                     I’ll talk about MDR in general, and then I’ll dive into what it means for big companies as well as startups.

Seth:                     So MDR is part of that change in safety, part of that changes and improvements that I think needs to be done coming out in 2020. There’s a lot of shifts going on, obviously, if people are talking about the notified bodies and how many notified bodies are there going to be. These are real issues.

Seth:                     You look at it, so I won’t repeat all that, that’s all out there. When you look at it, what does it mean to impact and how does it impact your business? It really comes down to auditability of my data and can I track all of the data that I’ve used to run my business.

Seth:                     That’s really what it is at the core. Again, very simple to say in one word, but in reality, how do I actually do that? And it’s one that we’re focusing on a lot here at Veeva and one that I think we’re poised to really help because you’re talking about how do I take this, my regulatory data, as clinical data, whether it’s for a clinical trial or post-market data that I get in the field. How do I integrate that into my clinical evaluation reports that now need to be updated more frequently?

Seth:                     It’s really the whole business, right? And that’s why I think people are really kind of starting to panic because I think a lot of folks were focusing just on one piece of the quality and then they realized they really need to think about how they’re managing their quality differently because now quality has expanded from my manufacturing space and now I need to take those core principles, that documentation and auditability and expand them across my business. That is some of the impetus and stimulus that has caused a lot of device companies to start looking at solutions such as Veeva.

Seth:                     It’s also, as I mentioned, a big part of why I think now for people to start entering this space next, [inaudible 00:29:30] we’ve been here for a while. We have 80 customers already that expand our presence in this space and put more focus on the products and solutions for device companies. Just makes a lot of sense, because unless you’re really thinking about a transformation and really changing about the way you run your whole business, you’re at risk, right? You’re a risk from data audits right here, which would then cost a ton of money. You’re at risk of being non noncompliant. Those are things that you, again, don’t want to be doing. You want to be focusing on innovation and bringing products to your patients. I think also a lot of people thought MDR might not happen, or it’s going to get delayed, but it’s happening and you’re not pushing it back.

Seth:                     It’s not getting delayed. Everyone’s keeps on saying this, but the mission is pretty clear, it’s happening. I think that’s also leading to a little bit of the panic. Everyone’s like, oh yeah, we have more time. You know, we’re not ready [inaudible 00:30:23] and it’s happening. All that together is why I think being MDR Ready or thinking about MDR has had such a big impact. It impacts all of your documentation, all of your product development processes. You have to document all of your distribution channels with UDI compliance, what am I doing around the world? Can I track my product? All my sales and marketing material, everything is impacted by MDR. When you look at the impact of small businesses versus large businesses, large businesses are definitely impacted more because of the number of products they have on the marketplace.

Seth:                     A lot of it is actually sales and marketing requirements and distribution are the big challenges for the big companies. The small companies are less impacted today, I would say in general, because they don’t have that, the distribution and the sales and marketing piece to worry about. The product development process is more similar in the back of mutation or on product development and the needs for MDR. While there are more to bring your products to market or you may have to have more clinical data, your CRs have to be more in depth, those are, I would say incremental as on the preapproval process. Whereas the sales and marketing, the distribution tracking is exponential increase of over what had to be done before. Big companies are definitely impacted more than a small startup, a small start-up or a small innovator, they need to be aware of those things.

Seth:                     The bigger challenge actually for the small company, while they might have a similar regulatory path or the regulatory requirements might be the same, again, maybe a little more clinical data, a better CR, the bigger issue for them is going to be, is there a notified body that that will take me on as a client? I think that’s actually gonna drive a lot of folks look more US, because the notified body bandwidth for small companies is really going to be tight.

Dan:                       Yeah. I understand a lot of notified bodies are kind of pulling back based on based on MDR requirements.

Seth:                     Correct. Yeah. There’s a couple who have decided not to be in that business anymore. I think we’ll get up into 10, 20, I think there’s a lot of folks that are notified bodies who have their applications in review.

Seth:                     We have two approved already, but at the same time that also might be an indicator of the quality of that notify body potentially. Were their systems already prepared for something like this to support that additional approach or documentation?

Seth:                     The big companies I think might’ve had probably had more, again, I’m just hypothesizing here, had more aggressive infrastructure and those things in place, so this transition, it was essentially not, not that it was easy, but a little bit easier. At least the costs to get compliant was, I think, very expensive for the notified bodies too. They had to absorb a lot of costs, train their staff, look at additional staff that they needed to hire to do these reviews. There’s a lot of work for the notified bodies as well, it wasn’t just filling out paperwork. They really had to transform what they were doing and managing their businesses too.

Dan:                       Sure. Cool. All right. Well thank you so much for making time for us on a a Friday afternoon in the summer. I think a lot of our colleagues are out on vacation and enjoying time at the beach. Thanks for making time to talk to us.

Seth:                     My pleasure, hopefully they can listen to the podcast on the beach somewhere, give them something to think about when they get back in the office.

Dan:                       I’m sure that’s everyone’s top priority.

Seth:                     Exactly. But this was fun, I appreciate your time. That was good discussion and hope we can do it again some time.

Written by Daniel Henrich

Written by Daniel Henrich

Director of Marketing at Archimedic

Medtech Mindset Podcast Funding Adam Dakin, Part II

EPISODE 10 – Securing Funding, Part II

In Part II of this two-part episode, Adam Dakin, Managing Director of Dreamit Health, covers funding trends in medtech and how to pitch to institutional investors. (Part I available here!)

Adam and Dan discuss:

  • Medtech funding trends and how they’ve changed in recent years
  • Investor perspectives on medtech vs. digital health
  • How to be build value to make your startup attractive
  • Tips for success at the pitch table

During this episode, Adam references some great resources available from Dreamit for startups preparing to pitch.

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Episode Transcript

Adam Dakin:   Yeah, I mean, so the reality of where we are today in the funding cycles, in the med tech spaces, the vast majority of investors want to see their money going toward commercialization. So while you might not necessarily be on the eve of commercialization, you haven’t hired sales guys, the manufacturing plants not chugging away for spitting out products and in creating inventory for three shifts a day. You might not be at that point, but investors want line of sight to that. They want to believe that my money is going to get you to that point and at least you will be funded for an initial market entry. So that varies widely, right? If you have a very simple widget, with a very straight forward regulatory pathway, it doesn’t cost a lot to manufacturer. Then that kind of accompany may very well be interesting. Whereas another company, it’s still going to take a lot more money to get to the commercialization point even though it might have it in really compelling market opportunity.

Dan Henrich:       Like this kind of an example we started out with. That that has a lot of moving parts, right?

Adam:   Right. And market adoption, especially if it has a big digital health component is a big risk, right? Showing that early product market fit in an incredibly competitive environment. That’s the other thing we didn’t really talk about, but digital health is ridiculously crowded. Because the barriers to entry are so low. Two guys and a laptop can open up a digital health company tomorrow. Can’t really do that on the med tech side. There’s a certain amount of capital that’s required to build stuff, test it, right? That’s why the digital health space is just ridiculously crowded with look alike products. And as an investor it’s very hard to differentiate what’s real and what’s not. So as a digital health investor, we almost have to have at least some reference. You have to have some referenceable customers to even be considered by a professional investor. On the digital health side, you actually need real revenue.

Adam:   You need one to two million dollars of annual revenue as a general rule to be seriously considered by any professional investor. Whereas the good news on the Med tech side, you can get funded a lot earlier than that. You don’t need that one to two million dollars revenue, but you need some compelling clinical data that this works in the hands of real users. So got to offer a little bit of a tangent there, but I think it’s an important point.

Dan:       Well, speaking of one and two million dollars of revenue, you know, so this last milestone that we have laid out in our outline here is your first commercial sales, right? Who’s investing then? Is that where you really start to attract a lot of competition, institutional investors because your acquisition potential is much higher or?

Adam:   Yeah. Well that’s the time at which … I mean once you have that line of sight to commercialization, and as an investor, that’s where I want my money to go. I understand some of my money will always go to continued product development, more clinical data, product line expansion. That’s all good. But I want to be in the market as fast as possible. So I want to believe that in most cases, not always, but in most cases that at least some of that funding will get you to the point of commercialization. Will get you, because that’s what the acquirers want, right? They’re not going to take a lot of market risk.

Adam:   That doesn’t mean you have to have a lot of customers. Those could be your clinical trial sites that convert from doing trials to actually being paying customers. Hopefully they like the product, they’ve already had a good experience with you. Sure. And you’ve already anticipated taking them through that purchasing process so they become your first customer and your first users. That’s a good strategy to use, but that’s what acquirers want to see.

Adam:   Somebody’s got to use it. Somebody’s got to be willing to pay for it. We haven’t really talked much about the reimbursement piece, but clearly depending on your product, if it’s not well reimbursed under an existing code or payment scheme, you might have to get new codes.

Dan:       Right, and that’s a long arduous proposition.

Adam:   That’s right. I mean, that is, in our broken, fragmented healthcare system, that is a long slog. Getting any kind of universal coverage for something is no matter how good your technology or platform may be, investors are going to be very … investors have been burned a lot on great technologies with really compelling clinical data that had a real patient benefit, but took years-

Dan:       For [inaudible 00:36:07].

Adam:   … to get universal coverage, including CMS. And no matter how good it is, people won’t use something if it’s not paid for it.

Dan:       Okay. All right. Wow. That’s a lot to think about, I think for our listeners, for sure. But maybe we can get into the nitty gritty a little bit more … like I said, you’ve been on both sides of the pitch table a bunch of times. And in fact, I think you’ve written some pretty good articles on what are the do’s and don’ts when you’re making … If you get to the point where you’re pitching to institutional investors, what are the common mistakes that med tech founders and entrepreneurs make in those pitches?

Adam:   Because there’s blocking and tackling, right? You need the right content, right? Can’t tell you how many companies pitch us. It’s like, “Where’s your competition slide? Oh that’s not here. Left that out. Oh wait, the market size, no slide there either. oh wait, clinical development plan, that’s not there either.” Those, while not sort of, you know, we call the record scratches, right? Those may not be mortal mistakes. They show that the team is unsophisticated.

Adam:   If you haven’t thought about these things and put them into your plan, what else haven’t you thought about? So it’s a little bit of a red flag. That’s basic stuff. Have the right content, make sure it’s defendable, have references to the sources in your deck. We’re going to challenge you aggressively on all your critical assumptions, right? You better have data to back up whatever assumptions you’re making, you better have data and sources to back it up. Again, very common mistake.

Adam:   A lot of entrepreneurs walk in, we call it the hand wave at Dreamit. The market is this big hands waving, right? Every doctor’s going to want one hands waving, and then that comes with a subtle … I can see the bubble above the entrepreneur’s head when we start challenging that says, “If you don’t see how big this market is, you’re an idiot.” Why don’t you see the vision that I see and believe what I’m telling you?” Because you’re not backing it up with data, right?

Adam:   If you’re going to say every doctor is going gonna want one, how many doctors did you talk to? How many doctors have actually used it? How many healthcare systems are actually purchasing it? Are you in contracting with a bunch of healthcare systems that convinces us that someone’s actually going to want it and buy it. If you don’t have any of that, you’re just making assumptions with nothing to back those assumptions up and we don’t bet on assumptions. Right. So that’s a very common mistake I think. I mean it’s all the classic stuff, right? I mean, some of this stuff is ad nauseum. Yeah, show us a big market, show us you have intellectual property, show us you’re a great team that knows how to execute. Those are all table stakes, right?

Adam:   If you don’t have those boxes checked, don’t bother showing up. Okay. That, that’s kind of fundamentals of what every venture investor will tell you. You gotta be a great team, right? Ad Nausea, management, we bet on management. We bet on the jockey, not the horse, all true, although all very cliche, right? At the end of the day though, we form impressions, first impressions, and I will tell you, I’ve asked multiple venture capitalists this question. They decide within the first 60 seconds, most of the time if you are a venture backable team. So you got one chance, they make that first impression and that’s why a thoughtful, cohesive pitch deck and done in the right way where right up front, right at the very beginning you are really making it clear what your value proposition is and how you’re differentiated from the hundreds of other deals most investors are looking at is critical.

Adam:   Because if you don’t do that, I guarantee you they will be reaching for their smart phones within the first two or three minutes and you’ve been put into the no bucket very quickly. One way to stay out of that no bucket is also make sure you’re super well prepared. Again, surprise. It’s like go into an interview. Would you go to an interview where you knew nothing about the company or the people who were interviewing you? Well, some people do and they probably don’t [crosstalk 00:41:09]. A lot of people do and they don’t get the job, I’m guessing, right? I mean, when a company is coming to a venture fund, it is very common at the very beginning for the fund to say, “So tell us what you know about our fund.”

Adam:   You should be able to say, “I know what deals you’ve done. I know what stage you invest in, I know what your profile is. There are these other companies in your portfolio that I think are very synergistic.” Yeah, we want you as an investor because you have expertise in this space. Oh, I know that two of your partners were on the board of another company that was very successful. We think we can really learn and benefit from folks who have that expertise, right? One, it has the virtue of all being true. And two, it shows that you did your homework before you showed up because a lot of companies answer that with really a morphous, “Oh, we know you’re Andreessen Horowitz and you’re such a great firm and we would just love to have such a brand.” That’s a very weak response.

Adam:   It shows you’re not well prepared. So walk into the fund, do your homework. Know who the partners are, know their backgrounds, know their other investments. Like everything in life, it’s all about preparation and then have that pitch tight rehearsing on other people, solicit critical feedback. You don’t go to Broadway with your first play, right? Go off Broadway. Pitch friends, family, then take it to investor, you know won’t invest. Let them throw tomatoes at you for a while. They’re probably not going to invest any way or just call in favors. “Hey, I know you’re not going to invest, but would you mind just giving me some critical feedback, point out the holes in our story and our pitch.”

Adam:   Once you’ve rehearsed it a bunch of times, and you feel like it’s tight and it’s game ready, then you want to get in front of the high potential targets who might actually invest in your company.

Dan:       All right. So I want to go back to something you said earlier about the importance of being capital efficient early in the process. That’s something that we run to a lot when we’re talking to early stage med tech entrepreneurs. They want to know that they can get as far as they can on that initial money that might be theirs and their friends and families and that sort of thing. But it seems like sometimes they want to be so capital efficient that they’re willing to sacrifice things like speed to market and they want to do an MVP, which is not the same in the med tech world as it is in the digital health world perhaps. How do you view that as an investor, that relationship between when somebody is emphasizing capital efficiency against other factors?

Adam:   Yeah. So I think you’re highlighting the point that these companies can often be penny wise and pound foolish, right? So capital efficiency is table stakes, but most startups by necessity are reasonably capital fisher, right? They’re not paying themselves market salaries, right? They’re not renting an expensive office space. They don’t have super nice office furniture. If you have those things, that’s a red flag. We do. We see companies where the management team is paying themselves ridiculous salaries. And like, okay, that’s a red flag. That is probably not a team that we’re going to be excited about investing in. Those really are more the exceptions than the rules because most founding teams realize that that capital needs to be used to develop the product, not for other perks. If you’re at a startup, you hopefully understand that you’re going to be making some financial sacrifices in hopes of a longer term gain.

Adam:   But that said, yeah, there are places to spend the money and those places include developing, well, let’s even roll it back further. The first step is actually understanding the problem you’re solving, right? And it is amazing to me, and I’m sure you guys see this at Smith wise, where a doctor or an adventure shows up with their widget and they’re like, “This is going to save the world. This is a problem that I face each and every day and man, I’m just so excited about this.” Well that’s not necessarily a market, right? Solving one problem for one doctor.

Dan:       Great data point. Where’s the trend?

Adam:   It takes three points to make a trend. I mean, you have to talk to a lot of customers and that may not just be the person who’s actually using the device in their hand. That probably includes who’s gonna pay for it, right? So the customer and that constellation of stakeholders that will touch your device. You need to talk to lots and lots of those people before you run off. Expend intellectual capital first to understand the problem that you’re actually solving and who you’re solving it for. Amazing. Like that sort of deep discovery phase. How many companies just kind of skip past that with the assumption that if we build it, they will come. That every doctor will want one. Trust me.

Adam:   I think that’s … you can not spend too much time understanding and really coming up with a great problem statement. Great companies generally have great problem statements because I will tell you in any healthcare system, if you’re not solving a big, and urgent problem that’s on the very short list of problems that somebody high up in the organization, once the south, you’re not going to get purchased. You might start the purchasing process, but you won’t survive it. It’s such a slog. You need so many champions to get you through that process, you will never survive it. So first it starts with really understanding the problem that you’re trying to solve …

Adam:   It doesn’t cost much to talk to people and really come up with a good problem statement, which of course will also define, well, help inform the features and specifications of the product or platform that you’re ultimately going to develop. Now, let’s say you’ve gotten past that and now you are ready to spend some real money on product development. And you’re right, the MVP concept, which I think is almost a bad way to describe it. I mean, we tend to think of it … I like to think of it more as a minimal viable experience as opposed to a minimal viable product because the bar is higher in healthcare. What you might call a minimal viable product into a healthcare system, but if they don’t like it, you’re done. And you’d be like, “But functionally it’s doing everything it’s supposed to be doing.”

Adam:   Yeah, but it took me 24 clicks and it took me 10 minutes to set up your device before I could use it. It’s not fitting my workflow. I really don’t care if you call it a minimal viable product, it’s a bad experience and I’m not using it. I think that concept sends, you know, people have a perception of what a minimal viable product is. That doesn’t mean it’s ready to put in the hands of potential customers, right. That’s a little bit of a divergence, but when you look at the other pieces of the business that are going to be critical. Intellectual property is always critical with medical devices, right? No one’s going to fund you if you’re not building something that a, they think you’ll be able to protect and keep as yours and b, you won’t infringe somebody’s else’s patents. Freedom to operate.

Adam:   So, yeah, that’s a place that’s worth spending money. Expensive lawyers. Yeah. You wanna, you wanna hire lawyers that have experience in your space. If you’re an ultrasound device, hire lawyers that have worked on an ultrasound devices. Just makes sense. Regulatory, same thing, right? If you’re a ultrasound device, hire regulatory experts that know that space, right? Not only do they have that pattern recognition from all the experience, but they also probably have relationships in the FDA within those people that assess ultrasound technology that’s going to facilitate the process for you. Those people are expensive. There’s no way of getting around it.

Adam:   Entrepreneurs cringe as I. When I hear the hourly rates that some of these consultants get, but at the end of the day, they’re actually worth it. So always tell entrepreneurs. Hire the expensive lawyers, hire the expensive regulatory consultants, hire the good product developers who know what they’re doing. I mean, there are a lot of product development firms out there that don’t really understand the medical side. They’re happy to knock out a widget for you, right? But does it meet all the standards? Will it pass electrical testing at the hospital? Will it meet the FDA standards when you finally are ready to put that 510K in? If the answer to those are no, you’re not working with the right firm.

Adam:   And that’s why firms like Smith wise are the places you want to go because you guys understand what those requirements are and yeah, guess what that costs more to develop then going to some generic product design firm that’s going to knock out a prototype that’s not gonna sort of … that effort won’t be translatable as you continue your development pathway.

Dan:       Right. Thanks for saying that, I’ll buy you dinner later.

Adam:   No, it’s really true. Look, I’ve done a lot of projects with you guys. This is not a paid advertisement. I’ve seen the difference with firms that do product development with companies that don’t have that depth of experience and it’s very shortsighted. It is less expensive in the short term. There’s an expression, right? There’s never time to do it right, but there’s always time to do it over. And it’s a lot of entrepreneurs who make that sort of mistake.

Dan:       Great. Great. And then we’re coming up on the end of the time we have set aside for this, but I do you have a question about leadership teams. Because I know that investors look very closely at the team that’s going to be guidance thing to market. Often I think we see in this space there’s a change in the leadership team as a product approaches commercialization. How do you view that and what are investors, excuse me, what an investor look for at different stages in terms of the skill sets that they expect to be part of the team that’s going to be able to bring this product to the next milestone?

Adam:   So the vast majority of startups have technical founders, right? That’s an engineer, that could be a doctor who brings the clinical expertise. But the commercialization expertise for the most part is not resident within the company during the early days of product development. And as investors, that’s perfectly fine. That’s what we expect to see. But again, back to the prior conversation that we are all about commercialization. What’s it gonna take to get there? What’s the go to market strategy when this thing gets to market? Who understands that? Who’s going to build that out and execute? We sort of see two scenarios. One is attractive and one is not. The one scenario is, “Hey, we’re, the founders, we’re the inventors, we’re super smart.” They probably are. “And we can take this thing, the distance. We’ll build it, we’ll sell it, we’ll do the marketing, we’ll figure out the go to market.”

Adam:   Maybe that’s true, but for the most part, those teams don’t have that skill set. Okay. So then one of two scenarios plays out. The company makes great progress. That’s awesome. It starts to have line of sight to commercialization. Great. And that team wants to hold on and do the execution and the investors say, “Hold up. You’re just not the right team.” And that can be a difficult conversation to have because at that point, the investors want to bring in outside expertise or senior level management team, even a new CEO of the company to say, “Okay, at this point the focus has shifted. We’re focusing away from the development, still very important, but we are all about getting this thing to the market.” The better scenario …

Dan:       And so should the technical founders be, right?

Adam:   Absolutely. They’re exactly right. Their vested interest is in seeing this seat succeed commercially. The better way to position this is for the technical founder to say, “We get that. We’re all onboard. We cannot wait for an awesome team that gets … but we get to that point where we have line of sight to commercialization. We realize we’re probably not the team to do that, so we will fully support engage with getting that management team in or those experts on board that can take the company to that next step. Like that’s music to an investor [crosstalk 00:55:33] when it’s sincere.

Dan:       That shows maturity and understanding of the industry.

Adam:   Exactly. Because every investor has countless war stories of a CTO or a founder who didn’t want to give up the reigns. And it becomes hugely problematic for the company in ways that some are obvious, but some are less obvious, right? It’s extremely difficult to raise capital for a company where there’s tension between the board of directors and the founders over this issue of bringing in the commercialization team because that’s going to become apparent to investors as they go through the due diligence process. And if it becomes apparent that that’s an actual diligence issue, it just gives us a reason to walk away very quickly. Like, we don’t want to peel back the onion and figure out who’s upset? why are they upset?

Adam:   We call it founder drama. It happens all the time. They’re not getting along. The founder’s vision for how this thing gets commercialized is totally different than the CEO’s vision or the board’s vision. We don’t want to figure out who’s right and wrong. We don’t have the time. We’re just going to walk away. So that alignment between, “Okay, we have this awesome technical team, they’ve really built an amazing product, but now we need to really think about the next step of the company is really important, and you’ve the board, the founders, the future CEO, they all have to be extremely well aligned.

Dan:       Yeah. Great. Well, I think we could continue this for a while, but you have some products to commercialize. So Adam, I really want to thank you for your time and I think this will be really, really good background perspective for our listeners to hear.

Adam:   Thanks, Dan. No, it’s a pleasure. I’m happy to do it.

Dan:       All right. Thanks.

Written by Daniel Henrich

Written by Daniel Henrich

Director of Marketing at Archimedic

MedTech Mindset Podcast: Securing Funding with Adam Dakin, Part I

EPISODE 9 – Securing Funding, Part I

In this episode, Adam Dakin, Managing Director of Dreamit Health, covers funding trends in medtech and how to pitch to institutional investors. (Part II available here.)

Adam and Dan discuss:

  • Medtech funding trends and how they’ve changed in recent years
  • Investor perspectives on medtech vs. digital health
  • How to be build value to make your startup attractive
  • Tips for success at the pitch table

During this episode, Adam references some great resources available from Dreamit for startups preparing to pitch.

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Episode Transcript

Dan Henrich:     Hey Adam, how are you today?

Adam Dakin:      Doing great, thanks.

Dan:       Hey, thanks so much for joining us. Funding is a topic that we wanted to cover early on in this series, almost every one of the med tech entrepreneurs we talk to is struggling to raise funding to get their project off the ground but before we get into it, maybe can you tell us a little bit about Dreamit and your role there?

Adam:   Sure. So real briefly, my background and thanks so much for this opportunity. It’s [inaudible 00:06:10] to chat with you. My background, I’ve been doing early stage health tech companies really almost since I got out of school. So 25 plus years started out in sales. But since then, I’ve co-founded five health tech companies, served as the CEO of three of those, raised a lot of venture capital across those five companies. Some of those companies went well, some of them did not. So I have both perspectives. Then, about a year and a half ago, I moved really from a career as an operator to the investment side. I joined Dreamit Ventures, which is a venture fund located in Philadelphia.

Adam:   Our focus is digital health and med tech. We’ve been around for over 10 years. We’ve worked with over 130 companies in the health tech space. Our model is a little bit different than traditional venture in that we run what you might loosely describe as an accelerator alongside of our venture fund. That accelerator exists for the sole purpose of generating deal flow into our venture fund. We only invest in companies that go through that program. We are super selective. We take 3% of companies in that apply to that program. So in the health tech [vertical 00:07:25], we work with about 15 to 20 companies a year. We have urban tech and secure tech verticals as well.

Adam:   Model is exactly the same in those verticals, but what is unique about us compared to other programs or accelerators is we don’t take a big chunk of equity up front. There’s no co-location involved. I prefer to describe us more as a sleeves up venture fund because we work very intimately with those select companies that come into the program and we are all about helping them acquire customers. We have an incredible stakeholder network of over 30 enterprise healthcare partners, payers, large multinationals, big Pharma partners who know how well vetted and well prepared our companies are. So they’re willing to engage very closely with those companies.

Adam:   We’re getting access to decision makers for them to accelerate commercial relationships. Then our second big value add is access to capital. We reach out to over a thousand venture funds each cycle. Again, those funds, no, we’re only bringing them the best of the best. So they look very closely at each cohort and then they decide which companies within that cohort they want to get face to face with. Most of our teams will get 15 to 25 face to face meetings with venture funds across a two week period that we call investors sprints.

Adam:   Our track record’s pretty good. Over half of our companies will close around within six months of getting through the Dreamit program and then we will call, invest in the vast majority of those programs. That’s pretty important for us because if we don’t co-invest, we don’t get paid. You’ve kind of gone through the program for free. If we never write a check that aligns interests very nicely between us and the founders of the company.

Dan:       Great. Great. So one of the reasons we thought you’d be such a great guest for this episode, it is just that fact that you’ve been on both sides of the pitch table a bunch of times. And so we want to just give people an idea of realistic expectations. What it’s like to be pitching your medtech company and how you have to think about the investor’s perspective as you go through that process. But maybe before we jump into the nitty gritty of what to do and what to expect in fundraising. Can we just talk about kind of trend of current funding and med tech and digital health and how has that changed if at all in recent years?

Adam:   Sure. The reality is it’s gotten tough for early stage med tech companies to raise capital. There are a number of headwinds that the space has faced in the last few years. There are fewer acquirers now than there used to be. When I started out 25 years ago, if you were orthopedics or you were cardiovascular company, there was a hit list of 20, 25 companies that would acquire you and they would acquire you relatively early. You could have just a limited amount of human data and maybe a little bit of IP around your concept, and the big guys were willing to come in and go, “We get it. You proved at least at works. We’ll take it from here. Here’s a nice check.”

Adam:   Yeah. You may not have raised all that much capital at that point. So exits in the 50 or a hundred million dollar range were still very pretty nice exits for your investors. They were still getting a nice multiple on their invested capital. So what changed? Well, a few things. First, there’s been so much consolidation in the med tech space that now if you’re orthopedics, cardiovascular or other spaces, there might be five buyers for you. Well, the real value creation comes from creating an auction. You get something far enough along that you can get several acquirers interested in buying you, and that’s what obviously bids up the price.

Adam:   So fewer buyers supply and demand. It’s just tougher to get the valuations and the exits that we used to be able to get. The other force is that these companies are waiting to buy things at much later stages, so they’re not willing to take a lot of that early risk. They want things de-risked much further than they used to. They’re willing to pay a bigger price for it, but they don’t want to take clinical regulatory market risk the way that they used to. That’s because they got burned. There were so many bad acquisitions of early stage med tech companies over the last 20 years that if you’re somebody in business development at a big company like Medtronic, do you want to take career risk on something that’s not really proven? Probably not. You don’t want to underpay for something that doesn’t work.

Adam:   You’d much rather overpay for something that does. So the mindset has really shifted. What are the implications of that? As investors, we know we’re going to be in it for the long haul, right? We’re not likely to get a quick exit. We’re going to … it’s going to be a much more capital intensive process to get that company to the milestones where it becomes, an attractive acquisition. So that’s one of the reasons why it’s gotten really tough for early stage investors, right? Assuming you’re not going to get an early exit. And that’s a very dangerous assumption that a lot of entrepreneurs make. We’re going to need a lot more capital along the way.

Adam:   So if you come in early, you are at risk for heavy dilution and it only takes one ugly financing along the way, to essentially wipe out or greatly diminish the equity stake for the early investors. As an early investor, you take clinical risk, you take product risk, regulatory risk, but you’re also taking huge financing risk because if that company has trouble raising capital in the next round, I mean worst case, they don’t raise capital, your investment gets wiped out or they raise capital, but they do it on what might be perceived as very harsh terms. You’re going to get heavily diluted, right? And your equity stake we’ll get either wiped out or dramatically reduced.

Adam:   So unfortunately those are some of the factors that have really made it less interesting. The other big factor is that large sucking sound you hear is the money moving over to digital health. Why is that? So digital health requires … It’s a lot less capital intensive. We just talked about med tech is capital intensive, right? If most medical devices, if I’m going to take them all the way from development, through clinical trial, through regulatory approval, through market launch, right? Those are expensive. There’s a lot of money to be spent before I even know if my product actually works. So I don’t even get to turn the first card over in terms of does it work and is their product market fit until I’ve spent significant amount of money probably over several years.

Adam:   That’s very different from software, right? A couple of guys who are smart with a couple of laptops can build an MVP type product pretty quickly. And you can assess that. So it’s been alluring for investors to go into a space where they think, “Oh, the time to market short, it’s a lot less capital intensive. These guys will be selling a few million dollars of capital there in the market. While that’s true, there’s a flip side to that, which I think a lot of investors who are health tech investors but maybe not experience digital health investors don’t understand because you give that back on the sales side, the sales cycles are very long in digital health. I mean it is not [crosstalk 00:15:25]

Dan:       This is only in the hospital systems and …

Adam:   It’s an enterprise … It’s a system sale, right? Medical devices generally have a relatively small universe of decision makers and it’s a very reasonably well defined process in terms of what the hospital has to do, which committees they have to go through, what budget you have to get approved in. So it’s not fast, but at least it’s reasonably well defined. Selling software to an enterprise healthcare system, we say when you’ve sold a one enterprise healthcare system, you sold the one enterprise healthcare system. The problem is it’s not a scalable sales cycle. It’s a constellation of so many different stakeholders that touch you because it’s software, right? So it might be the patient, it might be the family, it might be the head chair, the clinicians in the department. But it almost inevitably includes the IT department.

Dan:       Where things go to die.

Adam:   Exactly right. We call that the wood chipper in digital health, right? Because you see that long line down the hallway, that’s the line of companies waiting for their product to get integrated into the EHR. I was just talking to one CIO. I was asking him what’s the timeline look like? He said at a large Philadelphia based enterprise healthcare system, 12 to 18 months, if you need a full integration. Now that can be accelerated. If somebody high up once to move you to the top of the pile, it can be done more quickly. But if you just walk into the IT department and say, “We need this integrated.” And they say, “Great, we’ll put you on the list. We’ll talk to you in a year.” Because almost every healthcare system is doing some sort of large scale, Epic, Cerner, large EHR integration, and that’s where their focus, so helping a small company or a startup integrate, not on their priority list.

Adam:   I think that’s frustrating for a lot of investors who go in thinking, “Oh, this is software, this is a SAS type business model. Great margins. We’ll just run out to the market because this solution is so clever and innovative and solves a real problem.” Which it very well may. But the process of adoption is very slow because so many stakeholders have to weigh in. One of our companies in their CRM had 30 different decision makers that they were managing every single day to get through the sales cycle at that hospital. That’s a pretty heavy lift. And by the way, of those 30, five had veto power.

Adam:   So at any moment through that sales cycle, if one person raised their hand and said, “I’m out.” The sale was over. That’s like walking through raindrops. I mean, that’s a difficult sales process, which unfortunately a lot of investors don’t appreciate and ultimately that actually creates some tension between the investors and the management team, which may be a conversation for another day. But it suggests that entrepreneurs should be thoughtful about who they bring in as investors and who they have on their board.

Dan:       Yeah. So do you think there’ll be a pendulum swing back towards the middle or back towards med tech?

Adam:   I’m very optimistic actually because med tech solves [inaudible 00:18:37] there’s generally a clearly defined clinical problem. You’re targeting that. So yeah, I think …

Dan:       And once you show that your product can actually improve patient outcomes, it’s pretty straightforward type of business case to make.

Adam:   That’s right. I mean it’s easier to define the impact on outcomes. One of the things we talk about, not so much in Med tech is ROI, right? Return on investment. You talked to a digital health company, you cannot get 10 minutes in without saying what’s the ROI and what’s the impact on work flow? How does it fit the system? And how can you quantify if the healthcare system sends a dollar on you, they’ll get five back. We don’t really have those discussions in med tech so much because it’s really much more about the clinical outcome. And if there’s a really compelling dramatic patient benefit or provider benefit, they sort of stipulate that there’s an economic benefit.

Adam:   Now that said, there’s still a burden on companies to prove that medical economic benefit, but it’s generally a little bit more straight forward. So yeah, I think right now actually because of the forces we talked about, the reality is med tech company valuations have gotten very depressed. If I put my investor hat on, that creates an opportunity to invest in companies at what feels like relatively low valuations. The exact opposite is happening on the digital health side. The valuations have gotten, in my opinion, ridiculously inflated. Pre-revenue companies that we talk to have a swagger and an attitude around what they think their valuation should be before they sold one dime of product to anybody. And they are raising money at those valuations, which is great for them, for the founders, not so great for us as disciplined investors.

Dan:       Yeah. Okay. I think that’s a great way to frame this discussion. Can we talk maybe about ballpark valuations for a young med tech company. Before they reached their various milestones of de-risking their device and the way to market. Often when we talk with med tech entrepreneurs, they’ve really put their heart and soul into a particular project perhaps for for years but that gives them a very different and perhaps inflated perspective on the value of their idea versus how investors in the outside world are going to see the value of their idea and their project.

Dan:       Say we have a device, it’s going to come to market through a 510K pathway, but it’s connected. It’s got sort of maybe a digital health element to it. It’s fairly complex and it’s going to be say, used to remotely monitor a chronic disease. So it’s not a simple path to market. This is a pretty complex development process. You have that idea and you’re filing for your provisional patent. What’s that idea worth to an investor at that point?

Adam:   Right. So look, as investors, we get the fact that entrepreneurs are passionate, they’re all in. It’s a very emotional connection to the intellectual property or the idea that they’ve developed and they have a vision and hopefully that vision goes beyond the financial returns. It really is a commitment. I mean, we’re in health because we want to help people, right? That’s why most people come. That’s why most inventors dedicate themselves to these types of inventions. The reality is an idea and even a patent, and frankly, even in an early prototype, doesn’t have a whole lot of value from an investor’s perspective. That doesn’t mean it doesn’t have value. It has a lot of value, but investors are looking at things through a purely financial lens. At the end of the day, we’re going to put capital in and we’re going to take capital out and we want a significant multiple on that capital, right?

Adam:   So we want things de-risked pretty much all directionally pointing towards market adoption, right? What’s the process to … How much is it going to cost and how much time is going to take to get it into the market, and then what’s it going to prove that the market will buy it and use it? And the reality is an idea, even a patent and even a prototype doesn’t really help us de-risk that. What we need to understand is how much time? How long is it going to take? What is the process? What’s the regulatory risk? What’s the clinical risk? And then at end of the day, we’re really trying to figure out, well, you know, what’s the market adoption going to look like? So lots of factors come into that. How big is the market? What’s the potential profit margins on your particular product? What’s the sales cycle look like? Et cetera.

Adam:   Are there cost effective distribution channels for this stuff? That all comes into play. We see a lot of med tech stuff that’s really interesting, but it has no economic distribution channel, no way to get to the market cost effectively. That’s a problem, right? That’s particularly true for low cost accessory type items that have potentially a lot of value, but you can’t justify direct sales force to sell those products, which means you’re forced to find a channel partner on day one.

Adam:   Well, if you’re finding a channel partner, they’re going to take a big chunk of the margin, and they may or not be committed to effectively selling and marketing your products. So there’s a lot of distribution risk for those types of companies. There’s a lot of de-risking to be done. The idea, the prototype, the IP, that is the very beginning of a long journey of de-risking the technology.

Dan:       Sure. So it sounds like a VC firm obviously is not going to typically get involved at at this point in investing. So where’s that money coming from at that stage?

Adam:   When you’re at that stage, that’s founder money, that’s friends and family money who are generally investing in you. They believe in the team. Yes, they probably buy into the market opportunity and your vision, but at that point, as I said, there’s little of substantive value from a professional and investor’s standpoint. It’s really friends and family at that point. Once you get a little bit further and at least you have, let’s say, some bench data, then you can start thinking about grant funding. But again, you’re probably …

Dan:       So we’ll call that milestone two, maybe you have a working prototype proving out technical feasibility and you’ve got some bench data to maybe show that it meets the standards for the predicate device maybe.

Adam:   Right. Exactly. So that brings you to the STTR/SBIR potential, for funding to get it to that next level. Then where do you go from there? I mean, at the end of the day, most professional investors want some evidence that the product actually works and somebody’s actually going to buy it, right? In Med tech universe, that’s generally, not always, but that’s generally at minimum some compelling animal data. Really, it’s first in human data, right? That is usually the big trigger and by the way, concurrent with that first in human data, hopefully there are some clinicians who are nodding their heads going, “I used it and I really like it and it seems like it works.” That’s a huge de-risking milestone and we talked to a lot of companies who I don’t think they understand that they need to be laser focused on getting there on his little capital as possible because they’re thinking, “Oh, we got to get the 510K, we got to get regulatory approval, we got to do all these things.” And of course the 510K or the PMA is a very important milestone.

Adam:   This matter if it doesn’t work, like spend your focus and your limited dollars building a product that works and people love, right? You need to understand what the regulatory pathway is. Absolutely. If you’re not an expert in regulatory or there isn’t a really clearly defined pathway, you need to work with people who are experienced and understand how to build a regulatory strategy. But in the beginning, you have to be laser focused on building something that actually works and creating at least a small body of data to support its efficacy and safety.

Dan:       Yeah. I guess another important thing to point out there then is that if you have regulatory approval, that’s the FDA giving you your stamp saying this works to some level, right? You can treat a condition with this, but that doesn’t mean it works better than the standard of care. That doesn’t mean that that it works for an investor or for a clinician to the level that there’s market demand for it, right?

Adam:   Yeah, exactly right? So there’s two crucial [crosstalk 00:28:44].

Dan:       Let’s call that milestone three. You have regulatory approval but …

Adam:   The reality is it does not prove that it works. You can get a lot of 510Ks, with no clinical data whatsoever. I showed it was from a bench top standpoint, it’s equivalent to a predicate device. That doesn’t mean it works.

Dan:       I guess what I mean is that the standard right from FDA is if you get regulatory approval, that means the FDA said you’ve shown to our satisfaction that this is safe and effective, but that’s not … their standard of effective is not the same as what you’re saying that this device works.

Adam:   If you get a PMA, you are correct. You have shown to the FDA satisfaction that your device is safe and effective. If you get a 510K, you’ve shown that you are substantially equivalent to a predicate device. That predicate device may or may not safe and effective, but it was cleared by the FDA before 1976, you know, a strange set of laws, right? Kinda bizarre how this whole 510K system works and it’s all based on predicate devices. But I think your a bigger point is the important one, which is getting regulatory approval does not provide validation of market acceptance [crosstalk 00:30:03]. It doesn’t prove that people will want to use it. It also doesn’t prove at all that you’ll get paid for it. It’s a prerequisite. People won’t use it and you won’t get paid for it if you don’t have regulatory clearance. But the converse is not true. Just because you have that doesn’t mean people will use it. And that’s really the biggest de-risking component that institutional investors are focused on. That’s what they want to see.

Dan:       Okay. So say we’ve cleared milestone three, which is, we have regulatory approval and therefore we’re able to conduct post-market clinical data collection. Then is that the point at which institutional investors may really become involved and what do you call that from a serious perspective?

Adam:   Yeah, I mean, so the reality of where we are today in the funding cycles, in the med tech spaces, the vast majority of investors want to see their money going toward commercialization. So while you might not necessarily be on the eve of commercialization, you haven’t hired sales guys, the manufacturing plants not chugging away for spitting out products and in creating inventory for three shifts a day. You might not be at that point, but investors want line of sight to that. They want to believe that my money is going to get you to that point and at least you will be funded for an initial market entry. So that varies widely, right? If you have a very simple widget, with a very straight forward regulatory pathway, it doesn’t cost a lot to manufacturer. Then that kind of accompany may very well be interesting. Whereas another company, it’s still going to take a lot more money to get to the commercialization point even though it might have it in really compelling market opportunity.

Written by Daniel Henrich

Written by Daniel Henrich

Director of Marketing at Archimedic

MedTech Mindset Podcast: Staking Your IP Claim

EPISODE 8 – Staking Your IP Claim

In this episode, Gregory Bernabeo, Patent Attorney and Partner at FisherBroyles, covers intellectual property ground rules and special topics in the medtech space. 

Greg and Dan discuss:

  • Why a patent isn’t what (exactly) what you thought
  • Is my medtech innovation patentable?
  • Are patents valuable if I can’t afford to litigate?
  • Can medtech innovators protect their IP rights and publish their research?
  • What’s important when selecting a patent attorney for my medtech project?
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Episode Transcript

Dan Henrich:                     Hey Greg, thanks so much for coming in today to talk with us about IP and patent issues regarding medtech.

Greg Bernabeo:                My pleasure to be here. Yeah.

Dan Henrich:                     Before we get started, maybe you can just tell us a bit about who you are, your background, your position and the firm that you work at.

Greg Bernabeo:                Sure. Be Happy to do that. Well, thanks for having me today. I’m glad to be here to talk to you about these questions and issues today in intellectual property. It’s where I spend my time. I’m an intellectual property attorney, a patent attorney by trade. I’ve been practicing for over 20 years. I work as a partner at the law firm of FisherBroyles and my core of my expertise is patent prosecution.

Greg Bernabeo:                I’m a mechanical engineer by training, but my technologies span mechanical, electrical mechanical, computer hardware and software and is a very good fit for a lot of what we see in the medical device space.

Dan Henrich:                     Well, I’m so glad to have somebody who has both an engineering background and an IP background to talk with us about these things. So why don’t we jump in here and just start by talking a little bit about what a patent is in theory and in application. I think people conventionally think of a patent as a stamp of approval from the government to commercialize a particular product or technology, that’s not quite correct, right?

Greg Bernabeo:                Not quite.

Dan Henrich:                     Tell us your take.

Greg Bernabeo:                What is a patent? A patent is a grant from the government of course, and they’re territorial. A US patent has application in the United States. It gives you legal rights in the United States, specifically the right to exclude others from making, using, selling, offering for sale or importing into the United States the patented product or making use of a patented process. So ultimately it’s a right to exclude others, not a right to practice.

Greg Bernabeo:                And I think in some ways, this is maybe the least intuitive part of patent law, but the idea is that you can have an improvement to something that is patent worthy and yet someone may have a prior patent that’s broad enough to keep you from practicing your invention. And so there are slightly different analysis for determining whether what you have is patentable versus whether you have a right as they might say, to practice it, to use it.

Dan Henrich:                     Gotcha. Okay. And what about the various types of patents? I hear this is a utility patent, this is a design patent, this is a provisional patent. Can you talk to us a little bit about what the different aspects of it are?

Greg Bernabeo:                Sure. Absolutely. In this context, in the medical device field that we’re really talking about two different types of patents. Utility and design. So design covers the ornamental aspects of an article of manufacture. That’s the language in our law. The ornamental aspects are essentially how the product looks. Utility patent is really the other type of patent. The second type. Utility patent covers not particularly the way something looks, but more so how it is structured or how it works or maybe a process and how the process is used.

Greg Bernabeo:                It’s more about typically structure and functionality than appearance. And in a lot of ways a utility patent can be much broader than a design patent. A provisional is a utility patent concept. A provisional is not strictly speaking of patent, it’s a patent application. It’s a first step down the road towards utility patent protection. 

Dan Henrich:                     What are the elements that I have to demonstrate in order for my application to be granted?

Greg Bernabeo:                Essentially, what you have is new. It’s thinking about it a very high level, but the legal test are utility, novelty and non-obviousness. So what does that mean? Well, there’s a lot that we could probably talk about on that front, but it’s probably enough to say for any kind of device product that has a physical structure, utility is very unlikely to be a bar that you can’t overcome.

Greg Bernabeo:                In the field of medical devices, I think you’re a lot less likely to have the typical problem with respect to utility. You can almost put that off to the side. What you really need to be thinking about is novelty and non-obviousness. Novelty means your device is new. Nobody’s done it before, doesn’t mean not on the market. It means nobody’s done it before typically from a structural sense, and that means no one in the US, no one in the rest of the world. It’s a global standard as to whether your product is new, your invention is new.

Greg Bernabeo:                Non-obvious means maybe nobody’s ever done it before, so maybe it’s novel, but non-obvious means different enough from what someone has done before. If what you’ve developed is new and different than what anyone has done before, but it’s all such a minor and trivial variation that it’s a mirror obvious variation of what has gone before, patent law’s not going to give you a patent, but if you’ve made enough of a step away from what’s already been done before, then you can demonstrate that your development is not only novel but also non-obvious and that you’re entitled to a patent.

Dan Henrich:                     Okay. What about what is and isn’t patentable? For instance, if I’m a surgeon and I invent a new surgical technique that no one has used before, can I protect that for my institution or for my practice?

Greg Bernabeo:                Yeah, that’s a good question. I think sometimes you see different answers to this question, but my answer to this question is, yes those techniques are patentable. A surgical technique or method of treatment type of claim is generally speaking patentable. Generally, they’re not enforceable in the US against a surgeon or a doctor. Usually you find that those claims are somewhat disfavored because the thinking is, “Well, we’re not going to be able to enforce this method claim against the person who’s going to be carrying out the method, the person who’s providing the treatment.”

Greg Bernabeo:                But the truth of the matter is elsewhere in the world, methods of treatment are in some ways a little bit more patentable. And even here in the US there are reasons to have those claims. And one of the reasons is that a medical device manufacturer may be pursued because they’re contributing to or inducing infringement of the method claim by providing a device that can be used in the infringing method.

Greg Bernabeo:                It serves a strategic purpose, but to the extent people say those claims are in lay persons term invalid or you can’t get those claims, I think what they’re really referring to is you can’t enforce them against the practitioner because the public policy of making sure that you’re treated properly with the right treatment when you need it outweighs the patent interest. Nobody wants your doc running off for a patent license in the middle of your procedure.

Dan Henrich:                     Okay. All right. Can you maybe just take us quickly through the typical patent process? There’s a lot of terms that we hear. Freedom to operate, prior art, patent prosecution, request for continued examination, patent maintenance. Can you just take us through the process and explain where the main terms come into play?

Greg Bernabeo:                Sure, absolutely. The way I’d put those terms together is that you might normally start with a freedom to operate search or study or non-infringement study. What this generally means is non-infringement typically you know the patent and you want and determine if I make the product I intend to make, am I going to infringe this patent and hopefully you can come to a non-infringement conclusion. That might be one of your earliest steps.

Greg Bernabeo:                Freedom to operate search is generally a little bit of a broader term, meaning you’re looking at the field of patents more broadly and you’re trying to determine whether there are any patents out there that might be problematic for you, and when you find one you might do an infringement analysis and hopefully come to a non-infringement conclusion. So those terms are about understanding the rights of others before you move forward with your own rights or your own product.

Greg Bernabeo:                And when you’re looking at those patents that already exist before you came along, you’re looking at the prior art. That’s the term we use, the prior art, you might say the state of the art. You’re looking to a body of knowledge that predates you and it’s against the prior art that the novelty and non-obviousness of your invention will be determined. So you’re going to compare what you’ve developed to the prior art.

Greg Bernabeo:                When you start your own process, you’re trying to advance the ball with your own intellectual property rights, one of your first steps might be a patentability study. So you might go out, look at those patents and determine, regardless of whether you may infringe them and there’s freedom to operate, you might look at whether what you have is different enough that you’re entitled to your own patent, determine whether what you have is patentable. Then you may file an application and that’s where the patent prosecution process really begins.

Greg Bernabeo:                Patent prosecution is a little bit of an unfamiliar term. Prosecution used in an unconventional sense for most people, but what it really means is the process of applying for the patent and the back and forth communication with the patent office where you might say you’re negotiating the scope of your rights under the eventual patent, and so that starts with a patent application or a patent filing. And during the patent prosecution process, typically the patent office makes rejections and the attorney and patent applicant make responses to overcome those rejections. And if you’re successful at the end, you get a notice of allowance, which means the claims you’ve negotiated that define the scope of your rights have been approved and your patent is going to issue.

Greg Bernabeo:                And so when your patent issues, you get an actual physical hard copy with a nice seal on it and that is the paper documentation of your patent rights and it’s an issued patent. Along the way, you might have to go through multiple rounds of patent prosecution and you only get so many for your filing fee. And so they might at some point say, “We’ve given you as much review as you’re entitled to for your filing fee,” and you might have to request continued examination, which is more about the fee for continuing prosecution than it is about other requests.

Greg Bernabeo:                You pay the patent office to keep going. You get to your notice of allowance, your patent issues and post issuance. After the patent has issued, you have to pay maintenance fees in the US to keep it in force. And those are due in the US basically every four years after patent issuance.

Dan Henrich:                     The typical term for a utility patent as 20 years, is that correct?

Greg Bernabeo:                It is 20 years and it’s under the newer laws. It used to be 17 years, but under the newer laws it’s 20 years, but those 20 years are no longer measured from issuance. They’re 20 years measured from filing, but there are actually term extensions that are available for various reasons.

Dan Henrich:                     Okay. This is a question that came up was we were thinking through, what’s particular to medtech about this conversation we’re having. You’re going through this patent prosecution process with the US PTO, the Patent and Trademark Office, and you’re trying to convince them of the novelty of your idea. But many of the clients that we’re dealing with, and I’m guessing many of the clients you’re dealing with are going to take a 510(k) approval pathway through the FDA.

Dan Henrich:                     To do that, they have to then turn around and convince a separate federal agency that basically what they’re doing is not new, that it’s safety and efficacy, essentially how it works is the same as a product that’s already on the market or maybe a host of other products and they’re going to cite that as a predicate. Do those claims ever come into conflict your world?

Greg Bernabeo:                Well, I should start by saying I’m a patent attorney and not an FDA regulatory attorney. And so there may be FDA regulatory attorneys that are closer to that issue than I am, but I would say I haven’t seen that problem. I think what the best answer to that question is, is that the purpose and focus in meaning of same as the predicate device for safety and efficacy, it’s really a different analysis than what we’re talking about. We’re talking about novelty in the patent context.

Greg Bernabeo:                I think the FDA is really more focused on the impact to the patient and very often in the patent process. We’re not nearly focused as much on impact on the patient as we are on things like structural differences. I think the structure could be different and the impact to the patient could still be the same.

Dan Henrich:                     Okay. All right, well let’s talk a little bit about how your patent informs the rest of your business strategy. So if your patent is pending, you have filed the application. What protections do you have for your IP? Is it done at that point? Do you have to be worried about your intellectual property if you’ve got a good solid application that’s currently being prosecuted?

Greg Bernabeo:                A couple of answers to that question. Patent application is important for any inventor. It’s an important step because it can prevent the loss of your patent opportunity or the loss of your patent rights because you have only a limited window of opportunity in which to pursue patent protection. When you have something that’s new, it’s not new forever. And ultimately, if you sit on that development too long, your own work can be used against you in determining whether what you have is new in certain circumstances.

Greg Bernabeo:                Filing an application is important because then you are more free to go and talk to those potential commercialization partners because you’ve captured your IP in an application. At the same time, you’re not done, definitely you’re at the first step along the path towards an issued patent to having filed your application and you have not yet enforceable rights. You have inchoate rights. You have rights that are not yet mature. So you’ve captured your intellectual property, which is important because then you can more freely go out and talk to these commercialization partners without losing your patent opportunity.

Greg Bernabeo:                But you don’t have something that you can use at that moment to stop someone else from making or using your development. You need to advance the application through the issuance to have that enforceable right where you could actually sue someone and get a judgment that would pay you royalties or an injunction that would preclude them from practicing.

Dan Henrich:                     It’s still then probably very important if you’re having conversations in any detail with commercialization partners, potential investors or vendors that you have a non-disclosure agreement in place prior to getting into any confidential details. Is that correct?

Greg Bernabeo:                Absolutely. That’s getting a non-disclosure agreement in place is important for a couple of reasons. It’s not a substitution in any way for your patent rights, but it complements them and so by proceeding in a way such that you have a confidentiality agreement in place first, it’s supports your efforts in not disclosing your invention before you’ve filed your patent application or even afterwards.

Greg Bernabeo:                And it also creates an immediate contractual obligation on the other party, but you can hold them responsible to in terms of not using or commercializing or disclosing your technology, and that’s great because it’s an immediate contractual obligation when you do not yet have IP rights that you can use because you don’t yet have an issued patent. So it can provide you some measure of protection of a certain sort before you have patent right type protection.

Dan Henrich:                     A lot of our clients come from academic backgrounds, that might be part of a large research hospital or university health system and in those academic environments a lot of your progress is measured by how much you publish.

Dan Henrich:                     Publishing, there’s an emphasis on publishing research, but if that’s research that you’re hoping to commercialize, does that ever come into conflict and how should you try and negotiate that in terms of making sure that your IP is protected?

Greg Bernabeo:                Yes. This is definitely something that comes up quite often because there is pressure to publish and get it out in the hands of the public as soon as possible. That objective works in a lot of ways, contrary to the objective of the patent applicant, which is really keep it secret until you file the patent application. So really what you need to do or we do as attorneys working with our inventors who are sometimes faculty, we make sure that they understand that we can work best together when we coordinate our efforts.

Greg Bernabeo:                There is a way to play the game such that they can go ahead and publish and you can still file a patent application at least in the US, but you might trade all of your international rights for that publication. You’ll lose those international patent opportunities. The best answer to that question is why don’t we work together from the earliest point so that we can get a patent application on file for you before you publish a publication that might work against you and not every publication necessarily does.

Greg Bernabeo:                When the applicants or the professors or inventors are doing their job as well as they can and we’re doing our job as well as we can, we’re working hand in hand so we understand what’s going to be published and when, so we can build an IP strategy around that. My view is always that IP plays a supporting role for the business or the university or the applicants. And so we have to find a way to conduct ourselves that fits with the objectives, not to reshape the business processes so that it’s convenient for the IP process.

Greg Bernabeo:                So we play a supporting role and we try to tailor how we do and when we do what we do, so that supports what people want to do anyway. But we can only do that when we’re working together really from the early stages.

Dan Henrich:                     Okay. So what about the flip side of the equation where maybe an inventor is in a different environment where they know that there are competitors working to solve the same problem and they don’t want to tip their hand by filing a patent application which will become public. They don’t want to let their competitors know the approach that they’re taking to the problem. Does it ever make sense to hold off on filing?

Greg Bernabeo:                Yes, it can make sense to hold off a bit, but it’s very dangerous with respect to your patent opportunity, especially under the newer and relatively recent in the timeline of patent system laws that are first to file laws because if your competitor publishes before you file you’re out of luck really, your patent opportunity evaporates. The other part of my answer to your question is that, when you file your application will not necessarily be published and it certainly won’t be published immediately.

Greg Bernabeo:                In the normal course of events, you file a provisional or a non provisional application and the first publication is 18 months later. So you’ve got at least 18 months, even if you’re going the route of making it available through the patent process as soon as possible. If you are willing to limit your rights to the US only and not pursue foreign rights, which is not always the case, but it’s sometimes the case, you can actually file your application and never have it published as an application, it will publish only when you have an issued patent, only at the very end of the process.

Greg Bernabeo:                So at that point, your competitor may learn of what you’re doing, but you’ve already have your IP rights in hand. You’re a little more vulnerable when they see your publication and you don’t yet have your rights in hand and they can learn from what you’re doing and perhaps even make use of it for your patent issues. But so there are different ways to address those concerns.

Dan Henrich:                     Okay. We’ve talked about a patent has really a means of not so much as a license to commercialize or that you necessarily have the ability to commercialize an idea, but you have the right to block someone else from commercializing whatever piece of the process you have patent rights to. That all makes sense, but for a startup company almost every one of them is running on limited cash. They have a limited runway and they cannot in most cases afford to litigate against a competitor who’s infringing on their patent rights, especially if it’s a large competitor with deep pockets.

Dan Henrich:                     In that case, my question is what’s the real value of a patent if you’re in that environment where you might go through the patent application process and pay your fees and pay your attorney and at the end of the day you have a patent, but you can’t afford to defend?

Greg Bernabeo:                Again, a few answers to that question. So when you file your patent application, you’re not going to have a patent immediately. So not going to be suing immediately, but you have to capture your rights immediately or almost immediately because that’s the way the patent system works. There’s only so much you can do and keep your patent opportunity before you file a patent application. So the patent model really is file early.

Greg Bernabeo:                If startups had their choice, they would develop something, commercialize like crazy, see it’s worth a fortune, then take a little bit of that and put it in patent process. Unfortunately, that’s not the way it works. And the reason for that is the objective and in our constitution is to essentially accelerate the progress of science. So the model is, come up with something, just put it in the hands of the scientific community essentially as soon as possible so that the scientific community can learn from it and grow.

Greg Bernabeo:                That’s the reason why you can’t just sit on it. Part of the reason why you can’t just sit on it and then come back and do the patent process later. Patent process is really one that needs to be addressed very early on in order to keep that window of opportunity open.

Greg Bernabeo:                The other part of my answer is that you can do something short of litigating. Well, even before I give you that part, if you have a good position, you can find litigation finance companies that have business models of even particularly in the IP space, financing litigation and taking a piece of the recovery. So that’s another reason why, even if you don’t have all the money in your pocket, it may still make sense.

Greg Bernabeo:                You can also do something short of litigation. Sometimes something can be resolved by a demand letter, and you certainly don’t need the same budget you need for litigation to do that.

Dan Henrich:                     Like a cease and desist-

Greg Bernabeo:                Like a cease and desist letter. Exactly. And there can be some pretty stiff penalties for a competitor that knows that they’re violating your patent and continuing to do so. And that puts pressure on settlement even when you’re in the demand letter context. And you may have to go further to get there, but still there are reasons that someone who receives a demand letter may want to pay some close attention, particularly if they’re a big player.

Greg Bernabeo:                Another reason is that, if you don’t pursue those rights early on, that window of opportunity closes and it’s lost forever. And another reason is that by capturing that IP and establishing even an inchoate right, even you don’t have an issued patent yet, you have an application that has value. And so you can attract partners, commercialization partners, potential licensees, you can leverage or sell the patent application at least procedurally. And it has value as of the time it’s captured in.

Greg Bernabeo:                The one that maybe comes into play most often is that it’s part of a portfolio or part of a package that is a startup’s value really. It’s part of a startup and it can be used to attract capital into the startup, and oftentimes that is a motivator for a startup to want to capture their own IP. It may be that an investment in IP handling it in a diligent and thoughtful way and demonstrating that the startup has the wherewithal to execute in development and documentation and the patent process is a little bit confidence inspiring, that there will be further innovation and even the first one isn’t fully funded, there’s something there.

Greg Bernabeo:                And a lot of times IP does take somewhat of a meandering, or maybe it’s fair to say an iterative path, and so that there are not only a development, but there are also follow on developments that can be captured. So all of that weighs in favor of capturing what you have, and you have to do it in a thoughtful and strategically meaningful way, but I think the decision process is really not, if I don’t have enough millions of dollars to litigate then I shouldn’t file because there are a lot of other paths that don’t lead directly to litigation.

Dan Henrich:                     As someone who advises startups in terms of their IP strategy, do you ever take that iterative approach to say, “Okay, well this is what you need to demonstrate is patentable for your next round of funding. Let’s worry about claims, 2 through 10, further down the road after you have more capital.”

Greg Bernabeo:                Yes. Essentially, yes. There are a couple of ways to do that. One of the ways may be to file on a first application that has a scope that you’re able to pursue now even if you have to put some stuff on the back-burner. Putting it on the back-burner does have some risks. You can also file a broader application with the intention that it may be broader than what you can handle in a single application, but at least you’ve captured it and you can put it on the back.

Greg Bernabeo:                Back-burner meaning you can divide the application essentially into parts and pursue one part now and the rest of the parts later. And yet by making your filing, you’ve established an early priority date. You’ve captured it and essentially gotten a place in line at the patent office or in the state of the art, so that you could come back and pick it up later.

Greg Bernabeo:                So there are a couple of different ways that you can play that game so that you may have IP but limited resources and there are ways to plan for taking off a comfortably sized chunk and dealing with it sooner and deferring some of the rest. There are also procedural opportunities to try to take the slow path towards patent protection.

Dan Henrich:                     Okay. Let’s keep with that idea of a medtech startup that’s has a limited amount of cash. They’re looking to stay lean. Are there steps that, especially if someone is technically inclined, like an engineer, inventor or something like that, are there steps those folks can take ahead of engaging an attorney or a firm to prosecute their patent application to do preliminary work?

Dan Henrich:                     Is it worth spending time on Google patents or going through the US PTO database to try to do a solo prior art search or whatever? What can folks do to try to be in the best position they can when it’s time to bring on someone like yourself?

Greg Bernabeo:                I think the question is really focused at the very small end of the startup. Correct me if I’m wrong, but if we have someone who’s maybe thinking about striking out on with a med tech development in a startup mode, is there something they can do to begin to get the ball rolling? I think maybe one of the best piece of advice there is, yes, there are.

Greg Bernabeo:                And one of the best things you can likely do for yourself is make sure that you have a clear articulation of the development. And so before you see an attorney that will allow things to proceed much more efficiently. And so if you can prepare some text or description or even PowerPoint slides and drawings that would be fantastic. Even hand sketches can be very useful, but what typically is most helpful is a careful consideration of what the development is, why it’s being developed and how it works in a way that communicates it well in documentation.

Greg Bernabeo:                That usually works best. You don’t have to have it, but if you went to promote efficiency, that probably helps. And the exercise of preparing those documents on the inventors part is worth something in and of itself in that it forces them to think carefully about, “What do I have? Why do I think it’s novel?” Even in the absence of the prior art that can be very useful.

Greg Bernabeo:                Doing their own search can also be useful. That said, everything you find and touch need to keep track of because in the application process we’ll need to disclose things that are relevant to the determination of whether or not what you have is new and so the inventor will have an obligation, the attorney will have an obligation. And so a reasonably focused search can be helpful. Even better would be a patent attorney’s patentability search. And the reason for that is poking around on Google patents and doing word searches or poking around in the patent office website and doing web searches is not the same way that a patent attorney would typically search for a patentability search. We focus using a subject matter based and indexed classification system that categorize a subject matter in a way that is really independent or not so dependent of any particular words.

Greg Bernabeo:                Doing a word search is different than a classified subject matter search. So we can tend to get better results. But doing some searching on the inventors part I think is a valuable step and preparing drawings, I would say yes, that’s worthwhile, although any drawings that are prepared will be very helpful. Well done drawings as you might get from a Smithwise or someone else would be very helpful. I think what should be kept in mind is that very often those drawings will not ultimately be used in at least a formal patent application, they may be used in a provisional, but in a formal patent application, there are strict and varied drawing requirements that the patent office has.

Greg Bernabeo:                So it’s very unlikely that a lay person is going to produce drawings that are going to comply with the way the patent office wants to see it, but in terms of communicating it to the patent attorney, that can be very, very effective and they’re often sufficient. They’re often sufficient for at least a provisional application where those drawing rules are not applied in the same way.

Dan Henrich:                     We talked a little bit then about when the right time to begin the patent process then. You alluded to something earlier about the change, I believe it’s the American Invents Act set, the change from a first to invent to a first to file system.

Greg Bernabeo:                Yes, that’s right.

Dan Henrich:                     In light of that change, how important are keeping good records, lab notebooks, documenting the timeline of your development and all that sort of thing?

Greg Bernabeo:                I think you’re asking that question is the role of lab notebooks has changed somewhat with the coming of the America Invents Act, which did change us to a first to file system. So the American Invents Act has to some extent created a race to the patent office in a way that it didn’t really exist before. Because under the old system, the first to invent system, someone who filed later would not necessarily be a problem for you as the applicant if you were the first to invent because the determinations were made by who was first to invent.

Greg Bernabeo:                Now, the system doesn’t work that way anymore. It’s first to file, it’s first inventor to file. It’s really what it is, but someone else can pose a problem for you in terms of getting your own patent rights if you are not the first to file. Lab notebooks used to be used or the importance of lab notebooks in the patent prosecution process used to be use them to show that you were first to invent. So for a newly filed application, you’re not going to use a lab notebook to do that anymore because it’s not relevant in the way it was in the past.

Greg Bernabeo:                That said lab notebooks are still important and they’ve always been used for purposes other than preparing a declaration to show that you were first to invent as part of the patent prosecution process. It can be used for fundamental documentation to show that you are in fact an inventor, it can be used maybe to document something that ultimately is a trade secret, it can be used for a number of different purposes.

Greg Bernabeo:                The other thing that it’s more likely to be used for under the American Invents Act is to show that something is your own work and not derivation, it’s not derived from somebody else, which is a concept that’s more central to the American Invents Act. It’s a newer concept. I would say the answer to that question is they’re still very important. There’s no reason to discontinue any keeping have lab notebooks. In the patent prosecution process, they won’t be used in the same way that they’ve always been used, but they should still be kept.

Dan Henrich:                     Okay. This is a question that comes up fairly often, I would say with our clients at Smithwise. Many of our clients are perhaps clinicians or that’s the origin of an idea and so they are the original inventor, but then many of those folks go out and they hire a firm like Smithwise or an engineering firm to develop that concept further and those people are often gonna get involved prior to the patent application being filed.

Dan Henrich:                     Who needs to be listed on the application as an inventor? And is there a distinction between inventorship and ownership even if you’re going to sign the IP rights over?

Greg Bernabeo:                That’s a great question. This fundamental question of who’s an inventor comes up in a lot of different context and it comes up pretty often. Absolutely, inventorship and ownership are two entirely … Well, they’re two separate concepts certainly. And the question of who is an inventor it’s really a fact question. It’s governed by certain legal principles, but the question when you’re thinking about inventorship is who are those people who actually conceived of the invention? Who created it? Without regard to, are they in my company or somebody else’s company?

Greg Bernabeo:                The inquiry is just who contributed? Who contributed to the creation? Ownership is handled separately from inventorship. Ownership may be governed by contract or by whim. You may choose to assign it to someone without an obligation. And typically when a party like Smithwise is engaged to contract with inventors to do some development work, in my experience, it’s not uncommon that there will be ownership provisions in there sometimes.

Greg Bernabeo:                Ownership provisions in there and sometimes it will provide that ownership will be in the hiring party. And so ownership would be handled by an assignment document where the actual inventors sign a document saying, “I’m transferring my rights over to a company.” They’re two entirely separate issues. You absolutely need to not allow ownership to interfere with the inventorship determination.

Greg Bernabeo:                Identifying the inventors properly is very important for the integrity of the patent. Under certain circumstances when you’ve improperly named the inventors, it can be grounds for holding the patent unenforceable. It can be invalid essentially.

Dan Henrich:                     If you had advice to give, an inventor who knows that they need IP help, how would you advise them to go about finding a firm or finding an attorney or an agent to assist them with their application? What should be their criteria and what should their process look like from your perspective?

Greg Bernabeo:                Well, it’s definitely important to shop around because not all attorneys or all firms are equal. You need to find someone that you’re certainly that you’re comfortable with. I think what you should be shopping for is someone who has, I’ll say the right experience, but what does that mean? There are certainly going to be good patent attorneys at firms of all different types, small, medium, large, but what I think you’re looking for when you’re looking for a patent attorney in this space is someone with the right technical background.

Greg Bernabeo:                If you’ve developed something that’s a chemical development, you’re going to want a patent attorney with a chemistry background ’cause they’re going to best understand what your development is and how to present it. If you develop something that’s more electrical, maybe you need an electrical engineer, maybe software, you want someone who’s familiar with software, if it’s mechanical, you want a mechanical engineer.

Greg Bernabeo:                Although many of us because the projects are so intertwined with mechanical, electrical and software aspects you find that we practice and really across all those fields. But fundamentally you’re looking for a good technical match between your patent attorney and what you’ve developed. So you wouldn’t want a biotech patent attorney, you’d really want an engineer who’s familiar with the issues, if you have engineering in your device. That’s one of the first things I’d look for.

Greg Bernabeo:                Another thing I’d look for is experience in the medtech space. I think that’s also very important. Perhaps secondary to making sure you find the right technical match, but can be very important in ways that go beyond just the pure patent prosecution process. Also, want to think about the firm and how the services will be delivered and make sure that you have a good fit there as well. So again, not all law firms are the same. Not all attorneys are the same. You need to find someone you’re comfortable with.


Dan Henrich:                    You alluded to this earlier a little bit, but can you just tell us when would you say is the right time to involve a patent attorney or an IP firm for the first time? Is it when you have a napkin sketch, should you have a functional prototype? When should you go have that first consultation meeting with a patent attorney?

Greg Bernabeo:                I think it’s never too soon to have that initial consultation. I know that I’m always happy to talk to inventors or companies, startups even before they’re really ready to engage me. And the reason for that is, as we mentioned earlier, there’s a limited window of opportunity to pursue patent protection. Typically, in that first meeting we’re thinking about have any activities already taken place that could compromise patent rights? If so, when did they happen? What’s a critical date that we need to monitor?

Greg Bernabeo:                Or if something hasn’t already occurred or at least having a conversation about the fact that there is a limited window of opportunity and making sure that they understand what they should be keeping their eye on in terms of activities so that they can proceed in a cautious and thoughtful way that will preserve their rights and meet their goals. And so I think it’s never too early to have that initial consultation.

Greg Bernabeo:                Sometimes I find that I have an initial consultation, I get the client oriented in terms of thinking about what they should keep their eye on to preserve their IP rights. But I tell them, “You’re probably not going to need me until you get a little bit further along in articulating your ideas.” You don’t need to engage me. You don’t need to hire me until we get a little bit further along. Sometimes, if I feel that way, I certainly say it, but I think from the client’s perspective or from the medtech companies perspective, med device companies perspective, it’s never too early to have that conversation because time ultimately is working against you and you’d hate to find that you just missed your window of opportunity.

Greg Bernabeo:                You’d rather know about it and then you can decide whether to take advantage of it or not, but at least you can do it knowingly so it’s never too soon.

Dan Henrich:                     Sure. It seems like that initial conversation will be pretty important for a company that has just started to put together what is their IP strategy and how does it tie in when they’re presenting to investors, they would probably want to be able to say, “We’ve had preliminary conversations. This is our plan for when we’re going to file a patent if we haven’t already.”

Greg Bernabeo:                Absolutely. Absolutely. That can be very confidence inspiring and it demonstrates IP savvy and I think it can only be well received. Personally, I’m always happy to have that initial consultation at no charge.

Dan Henrich:                     Great. Well, we’ll make sure to post your contact information on the blog when we put this episode up.

Dan Henrich:                     Great. Thanks so much. I really appreciate.

Greg Bernabeo:                Thanks you. I love talking about these topics.

Dan Henrich:                     All right. Thanks.

Greg Bernabeo:                Thank you.

Written by Daniel Henrich

Written by Daniel Henrich

Director of Marketing at Archimedic

Overcoming Pediatric Device Innovation Challenges

EPISODE 7 – Overcoming Pediatric Device Innovation Challenges

In this episode, Matthew Maltese, Executive Director of the PA Pediatric Medical Device Consortium covers why it can be so hard to bring devices to market for kids and what we can do to help fix that. 

Matt and Dan discuss:

  • Current barrier to pediatric device innovation
  • How pediatric specialists operate without pediatric devices
  • Risk/Benefit rationale for small patient populations
  • Current industry and FDA initiatives to bring more devices to market for kids

Please note: We reference the Biodesign textbook in our conversation as a great resource. It’s available for purchase on Amazon here

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Episode Transcript

Dan Henrich:     Hey, Matt.

Matthew Maltese:          Hey.

Dan Henrich:     Thanks so much for being our guest today. I’m really glad to have the opportunity to talk with you about pediatric devices and how we bring devices to market for small patient populations. I think you and I met for the first time last year at Children’s Hospital of Philadelphia at an event for FDA reviewers-

Matthew Maltese:          That’s right.

Dan Henrich:     … To understand what are some of the challenges for pediatric devices coming to market. I wanted to maybe take some elements of that event and those conversations and package them into an interview between us for our listeners, who may not be familiar with those challenges. Can you tell our listeners a little bit about why is it so difficult sometimes to bring pediatric devices to market and why are they different from devices for adults?

Matthew Maltese:          The challenge with pediatrics is that there are technical challenges associated with it. The growth of a child throughout the intended use of a device can be challenging, particularly for implantable devices. You can imagine a heart valve, for example. There’s wonderful unmet need potential for anyone who can develop a heart valve that’ll grow with the aorta or the other great vessel that the valve needs to go in.

Matthew Maltese:          There are those technical challenges, but then there are simply financial challenges. I’ve given talks around the country on medical devices and kids, and I will often ask the audience. I’ll ask them, “How many of you have parents?” And everybody puts their hand up, right? Everybody’s got a mom or a dad, or a mom and a dad. Then I ask, “How many of you have children?” A smaller subset of the group will put their hands up. Then I ask, “Okay, for everyone who has both parents and a child or children, if you had a choice to develop a medical device or other therapy or pharmaceutical that would save the life of your parent or save the life of your kid, who would you pick?” Uniformly, who would they pick, Dan?

Dan Henrich:     I’d pick my kid.

Matthew Maltese:          You’d pick your kid.

Dan Henrich:     Sorry, Dad.

Matthew Maltese:          Everybody picks their kid. Your dad would pick your kid too. Everyone uniformly chooses their kid. However, as a society, it doesn’t always work that way. In fact, it rarely works that way. We know that the marketplace for adult products, particularly, you take orthopedic products for the hip and the knee and elsewhere, there’s so much volume there. So many cases and so many devices to be sold that that’s where much of the attention goes.

Matthew Maltese:          It can be just very difficult to draw attention to the kids, because the populations, as you put in your opening remarks, are small, meaning there are few in the population in addition to be individuals in the population being small, physically small. That there are few in the population and so there can be challenges because the upside from a capitalist perspective is not as big. However, there’s still an upside. I think that’s there’s still an upside in most devices for kids.

Dan Henrich:     Are there VC firms or angel investors who specialize, then, in small population or pediatric devices?

Matthew Maltese:          There are. There are some firms that have, I guess, identified that this is something that they are interested in. More often than not, it’s individuals. You mentioned VC, so if we think about the stages of investing, the early round, the seed round, where individuals are involved who have enough financial resource to get something off the ground and enough business sense to identify a business opportunity, that’s where you’re most likely to find traditional investment, a willingness for traditional investors to get involved.

Matthew Maltese:          Venture capitalists, in the strictest term, are often spending somebody else’s money. They can’t really allow, just by their duty, they can’t allow these emotional matters to come into play, unless it’s part of their stated mission of their fund. Just as an aside, I’ve been working in this field for quite some time, and I’m impressed to find many, many individuals who have the means to invest and have some sort of connection to pediatrics. Maybe a child who was a pediatric patient or a sibling or a child who is a pediatric medical provider of some sort, and they are touched personally by this and therefore are willing to invest in some way.

Dan Henrich:     Given, then, the fact that there are many fewer options for a pediatric specialist when it comes to treating their patients, what does a pediatric cardiologist or a surgeon or anesthesiologist, how does he or she navigate that in terms of treating their patients with the devices available?

Matthew Maltese:          I once asked, I wanted to find out in my own hospital, the off-label use of medical devices. Of course, off-label means it’s outside the range of the FDA approved range for the device to be marketed. The uniform response was it was easier for my clinician colleagues at the time to make a list of the devices that are used on-label. That was the response almost uniformly. That’s how they do it. They patch, they cut, they modify when the pediatric specific device is not available.

Matthew Maltese:          That said, there are examples of pediatric devices coming to market even now. Where manufacturers who are being good citizens or recognizing market potential or a little bit of both or mission driven and can make something work financially, they will make their products, they will modify their products for the pediatric space.

Dan Henrich:     So, then, pediatric specialists, many of them are forced to sort of become device innovators on the fly, it sounds like. So I understand correctly and our audience understands correctly, if you have an off-label use, what that means is that the FDA has approved the device for certain types of use that are on the label. The manufacturer may not market it for anything but on-label use, but physicians can innovate where necessary to treat their patients using, basically, an unapproved use for a device that’s on the market. Is that right?

Matthew Maltese:          That is exactly right. A great example is cardiac stenting in pediatrics, where most of the pediatric stents are biliary stents from the adult market used off-label.

Dan Henrich:     How do physicians begin to appreciate whether a particular off-label use is an acceptable level of risk, then?

Matthew Maltese:          Oh. You know, I’d have to say that I’m completely unqualified to answer that question.

Dan Henrich:     That’s okay.

Matthew Maltese:          I wouldn’t answer that question. I think [crosstalk 00:09:27].

Dan Henrich:     We can cut it out.

Matthew Maltese:          You’d have to talk to a physician, but also, it’s going to vary from physician to physician and by the risk of the nature of the device.

Dan Henrich:     If we think about the fact that I’m sure FDA recognizes that it is ultimately, in the long run, better for the patient to have a device that’s gone through that learning process of is it acceptable risk benefit ratio for use in pediatric population through a regulatory pathway and through clinical trials, versus physicians who are doing what they need to do to treat their patients with the devices that they have. Is there anything going on at the agency to try to make that traditional pathway to get devices approved easier or less expensive or faster?

Matthew Maltese:          That’s a great question. There’s a new word out there, a new phrase. It’s called, quote, the New FDA. There really is a difference between the FDA of only five or 10 years ago and the FDA we see now. I think the things that I’ve observed myself and heard from others is much more collaborative, particularly at the pre-sub phase. Much faster. I think it’s been well documented that they can turn around approval evaluations much faster than they have in the past. It used to be that the standard was to go to Europe and get the CE Mark and then come back to the States for the FDA approval.

Dan Henrich:     For pediatric devices specifically or for devices in general?

Matthew Maltese:          In general. Very recently, I ran into a company from Norway working on a cardiac product for peds, incidentally, that was coming to the US first, because they just viewed it as a faster pathway. I think that there are great reasons to be very optimistic about all medical device development in the US market. That just extends to pediatrics. Let me just extend that a little further and say that there are specific people in the FDA and programs like the Pediatric Device Consortium program and other programs that are really designed to foster devices for kids, so there’s even extra reason to do kids first in your device idea.

Dan Henrich:     Can you tell me a little bit about the consortia? I know that you’re director, is that right, of the Pennsylvania Pediatric Device Consortium?

Matthew Maltese:          That’s right.

Dan Henrich:     Can you tell me about what those organizations are and what their mission is and how they work?

Matthew Maltese:          I can speak for our own organization, but I think in general the mission is to bring pediatric medical devices to market, period. That is the mission. As our consortium, the Pennsylvania Pediatric Medieval Device Consortium, we don’t care where they come from. They don’t have to come from the Philadelphia region, even though we’re branded Philadelphia, Pennsylvania. In fact, most of our devices that we’ve worked on come from outside of our region. We always just sought the best devices for kids and provided them with modest funding but hopefully better in kind resources to help them move their products to a point where they can get further funding and eventually make it to market.

Dan Henrich:     How many consortia are there?

Matthew Maltese:          There are five total in the United States, including ours in Pennsylvania.

Dan Henrich:     What about other initiatives at the agency? I know there’s a program called Humanitarian Device Exemptions. I know there’s a lot to talk about how real world evidence may be able to inform the approval process for new pediatric devices and making off-label uses on-label.

Matthew Maltese:          I could tell you what I’ve observed. I can also point you to someone at the FDA who might be willing to talk to you and can speak more, just has more knowledge on what all the FDA offers. A good example, though not pediatric specific, but I think something that will benefit pediatrics in a very big way is additive manufacturing, also known as 3D printing. The FDA has put a tremendous amount of effort into just understanding how additive manufacturing plays into the medical device market, because much of the value propositions for pediatric or other small volume populations pivots on the volume. For example, if you have to make something out of a polymer and injection molding is your manufacturing method, the molds alone can be tens of thousands of dollars.

Dan Henrich:     And depending on the size of the patient, you may need how many different sizes, right?

Matthew Maltese:          How many different sizes? Maybe only a handful per hospital per year or per month, but you still need them. 3D printing offers the great opportunity of being able to manufacture in very small lots. You can even envision the concept of a vending machine, if you will, that produces and sterilizes and packages a custom-sized medical device from raw materials and sits either at a centralized location close to several regional small population hospitals, or even in the hospital itself. So there are, I think, tremendous opportunities in additive manufacturing. That’s just one area that the FDA is working in, and there are many others, many others.

Dan Henrich:     What about all the talk around real world evidence? I know that in September, I think it was, you and I were both at a symposium that Children’s National hosted in Philly talking about real world evidence.

Matthew Maltese:          Say it 10 times fast.

Dan Henrich:     And how it may be able to inform and accelerate the device approval process for pediatric devices. Can you explain, what is real world evidence and how it might be able to …

Matthew Maltese:          Sure. Real world evidence is exactly what the name implies. It’s evidence or data or information that is gathered from real world experiences. To contrast what perhaps that means is real world is not the experimental world, like we might do on a bench top or with an animal in a laboratory, or real world is not what we might do in Insilico on a computer with various simulation packages that are available for simulating the laws of physics virtually. Real world is real world. Real patients experiencing real medical procedures with medical devices and all the other therapies that surround it.

Matthew Maltese:          I think what has really launched this is the electronic health record and the potential for connecting devices and in some cases the rich information that the device collects. You think about cardiac pacing now, where each device not only paces the heart but collects information at the same time. And connecting that back to the patient health record, which is then integrated into everything that that patient has experienced from a medical perspective throughout their course of care. That has great promise. I think, frankly, it’s something that we’re going to look back on and we’re going to be able to define much better years from now than we can define it right now, but the potential is great.

Dan Henrich:     Is the main appeal of that, then, that you already have these devices that pediatric surgeons and cardiologists and others, they’re designed for adults, they’re being used for children, and if we can collect that data on the off-label use, then perhaps we can use that data in lieu of or to make a clinical trial to get an on-label use approved?

Matthew Maltese:          That is one example.

Dan Henrich:     What about actually developing new pediatric devices, then? How would real world evidence inform that?

Matthew Maltese:          Well, I think the development of a brand new device that is being used for the first time will follow the traditional pathway of real world evidence generation, which is the clinical trial. That has been in place and will always be in place. The things that I talked about with regard to the electronic health record will presumably make those clinical trials easier or more informative or both.

Matthew Maltese:          There might be a way for this enhanced medical records to improve epidemiological understanding of disease in ways that reveal more information about unmet needs, and then spawns the development of new devices. I remain convinced that the best way to discover unmet needs is for innovators to be involved in the practice of medicine or close to the practice of medicine. That can be, for a practitioner, practicing medicine and, for an innovator who’s not a practitioner, being close to a practitioner who is practicing medicine and physically in the room when it’s happening so that they can observe what’s going on from a holistic perspective. And spending time with the patient, and spending time with the payer so that they understand fully what the unmet need is and how to intervene.

Dan Henrich:     So, then, could real world evidence uncover potentially larger markets than appreciated and mean that the traditional pathway to device approval is more viable for investors? Is that kind of the thinking behind that?

Matthew Maltese:          Most certainly. I think when investors, or I should say, when medical device innovators or even those who are working within large medical device companies who wouldn’t really consider themselves innovators, but maybe advocates for certain types of technology being developed within those companies, can look to real world evidence to help them justify to their own management a particular direction or course that they have to take.

Dan Henrich:     Something else I wanted to ask you about, this is a little bit of an ethical quagmire, but there is an ethical discussion going on when it comes to children and other vulnerable patient populations. There’s one side of the argument might say, really, we need lower regulatory barriers and less scrutiny for these devices because there’s such an unmet need that having something is better than having nothing, even if there’s a greater amount of risk. Whereas on the other side, and both sides of this argument are very understandable, I think, people say, no, since we have children who are not making these decisions themselves, they are unable to appreciate the risk, we actually need greater scrutiny, greater regulatory thresholds for safety and perhaps efficacy than we do for adult …

Matthew Maltese:          Great question. Maybe just a short story before I answer that kind of shook me at the time. It really brought reality to how I thought about my role in the world. When I was young and starting in the field, I was at an FDA meeting where we were discussing medical devices and medical devices for kids and the various medical and scientific aspects of it, and we were talking statistics and p-values. The kind of thing that makes geeks just drool at the mouth.

Matthew Maltese:          It was a public meeting, and a parent stood up and went to the microphone and said, “I have two kids, and they both have the same rare genetic condition. One of them has died, and the other one, who is two years younger than the one that just died, is going to die. We need to just take action. We need to do something, because their death sentence is already written.” I remember it very, very clearly.

Matthew Maltese:          I think that stuck with a lot of people in the room, and that situation that I just described, I think, has been rehearsed many times with FDA regulators who have had the challenge of trying to field that sort of a plea from the public, a plea from a parent who’s going to lose their child. No matter what, inaction means my child dies. And try to reconcile that with the law. It’s very challenging.

Matthew Maltese:          Fast forward to just about a year ago, I was at a conference where the concept of patient preference was being merged with statistics of efficacy. What a patient defined as risky is maybe completely different than what the p-value, if you will, which is a measure of statistical significance and it can be used to determine if one course is more risky than another course. How to merge those things together.

Matthew Maltese:          In kids, it’s a bigger challenge, because many of them just simply can’t talk, and then those who can talk, they really may not be able to … They certainly can’t express themselves in a legally binding sort of way. You can’t enter into a contract with a minor. So the parent has to be in place. But there is a template here for getting patient preference from kids. When we do any kind of medical study, research on kids, it doesn’t necessarily have to be medical research, we have to pass through the institutional review boards. If a kid, depending on where it’s being done and how the local IRB panel has determined, there’s an age of assent, which is a child can’t give consent, but they can give assent. They can say, “Yes, I want to participate,” or, “No, I do not want to participate.” Then the parental consent is of course what decides.

Matthew Maltese:          That’s an evolving space as well, where it’s clearly been determined that there is not a one size fits all measure of risk. It depends on the population, it depends on the disease, it depends on the intervention that’s proposed. And most importantly, it depends on the preferences of the patient as to the type of life that they want to live with or without the intervention.

Dan Henrich:     I would imagine that conversation is very different depending on whether you’re talking about a life threatening situation or a condition which might mean paralysis or some other type of very debilitating, ongoing condition, versus something that we wouldn’t call it elective in the adult care setting, but something where the consequences are much less significant. How is the idea of this risk to benefit ratio evaluated? Should the conversation in more dire situations really be about not risk first versus benefit, but benefit versus risk? Does that make sense? Which of those things should be prioritized in the more dire situations, I guess?

Matthew Maltese:          I don’t know. It really depends. It really depends. I think there are people more qualified than I to comment on the situation. I’m an engineer. I’m responsible for building the intervention. I always have to keep in mind the ethics of it. Having the right people in the room when those decisions are being made, the clinical care team, the parents, the child, the patient. That’s really critical, and that’s where the decision has to be made. That’s at the point of care.

Matthew Maltese:          Taking a step back to the point of FDA approval, I think it’s the same sort of template. You have to have a panel that represents the clinicians who are experts in the field. You have to have somebody who understands the regulatory pieces and what the statutes and the law say. Then you have to have the patient, and in the case of kids, the patients and their parents, a panel of them or a body of them, who are collectively speaking about these critical issues. Of, “I see what the mathematical risk is, but this is what it means to my life.”

Dan Henrich:     When do humanitarian device exemptions come into play in those types of situations? Can you talk a little bit about what an HDE is and what type of situation the FDA might grant?

Matthew Maltese:          I don’t have a lot of personal experience with them. There’s a certain threshold in terms of patient population, that if it’s below that threshold then an HDE kicks in. But still, it’s a challenging pathway to go through. If you really want to talk to somebody about that, you’ve got to talk to somebody like Seth Goldenberg or somebody like that. He could describe very well the ins and outs and advantages of all the various pathways. It’s a matter of debate, too, ongoing debate between the industry and the FDA as to what those thresholds, in terms of patient population, should be set at.

Dan Henrich:     I hope we’ve done a good job of framing for our listeners what is this environment and what are the different struggles and trade-offs that innovators are dealing with when they’re trying to develop new devices for kids. You’ve mentioned a couple times how important it is to have clinicians either innovating themselves or to be very closely tied to the team that is developing this product. It would be interesting for me to understand better, how does a clinician who’s practicing medicine full time, most of them got into that for a very specific reason and they want to be, whatever their hours are, not 9:00 to 5:00, probably. They want to be every day hands-on helping kids and their families. What’s the model for a clinician innovator who, maybe, is using a device off-label for years and developing their technique and really seeing, in a way that no one else can, the potential for a pediatric device innovation? What’s the model that you’ve seen be successful for bringing that idea to market?

Matthew Maltese:          Let me walk back my earlier statement about clinician innovator. There are certainly great examples of clinician innovators, but maybe introduce a new concept called a clinician needs finder and decouple that you have to innovate and find the need at the same time. You could very systematically, as a clinician, spend time just understanding the need and recruiting others who may join you in the innovation process, the solution process downstream, but at the moment that you recruit them, you’re in the needs finding space of just trying to figure out, what is the problem? Because there are scores of devices and other so-called great ideas that die downstream because the upstream unmet need was either not there or not well defined. Spending a long time on understanding the problem and understanding the unmet need is always warranted. You heard it here first, folks. Clinician needs finder. It’s a new person. It’s a new title. The next part of your question was, how does a clinician innovator go about innovating?

Dan Henrich:     Well, what’s the model you’ve seen be successful in your experience or even, maybe, now I want to refine my question now that you’ve said that. You’ve spent a lot of time working in an environment with pediatric specialists. They’re aware of these needs. What’s the mechanism for collecting all those needs at a big research institution? Is there a method, does it vary from institution to institution? Or is it on the clinician to go to the biomechanics research department or whatever it is and say, “Hey, I have this problem. Can you help me solve it?” Or is there a mechanism for collecting those needs?

Matthew Maltese:          I think that there is not a mechanism, at least in my observance at multiple institutions. There are a few spots that do it well. The Stanford Biodesign program I think is excellent, and Cincinnati has a great program, and others too. I think that, for the most part, the clinician needs finder is not a frequently observed phenomenon. It’s mostly the clinician innovator, who hopefully starts out as a clinician needs finder and then blossoms as an innovator.

Matthew Maltese:          I’ve also found that clinicians are, in many cases, pretty good engineers. There’s a little engineer inside every clinician, and perhaps there’s a little clinician inside of every engineer. What I’ve experienced, it’s not the rule of law. It’s not how the universe must work. It just seems to be how the universe has worked that I’ve observed, if you will. I think some things that I’ve observed that I think are positive is that there’s now a trend where clinician innovator is an academic path. Do you understand what I’m saying?

Dan Henrich:     Mm-hmm (affirmative).

Matthew Maltese:          Just to give a contrasting example, at my own institution, the master of science in clinical epidemiology was a common degree, master’s degree, that was sought by clinicians following med school. There’s an emerging pathway of clinical innovator, almost like an equivalent to that, that is now gaining recognition in the academic setting. I think the more that that happens, the more that the traditional professional promotion standards and pathways recognize innovation as a legitimate academic pursuit, that we’re going to see a lot more clinician innovators come to be. Some are starting it in med school. I can’t imagine that, myself. I can’t-

Dan Henrich:     How you could juggle those things, right?

Matthew Maltese:          Yes. If I could think of a time when someone doesn’t have any spare time, it would be medical school. What I’ve learned is that there are times in medical school, particular years, that clinicians in training have time and choose to invest their time in innovation. Then they maybe step away from it while they go through the more intense portions, and then they return back to it as they move on in their career. I think, as I talked about the FDA and the future being bright there, I’m also very optimistic about innovation being a more intricate part of academic medicine and people’s careers as faculty and med schools.

Dan Henrich:     Putting aside the need for more clinician needs finders, maybe we’re going to call them that, not necessarily clinician innovators, but what is the path that you have seen for a device to move from an idea that a clinician has or a need that a clinician has and an innovator who has a potential solution, to getting the funding to go through regulatory approval and get, eventually, matched up with a manufacturer or whatever that might be?

Matthew Maltese:          Persistence on the part of the innovator. I think that’s the one thing, persistence. Less brilliance, more persistence. Maybe this is just because it’s fresh on the brain, but I’ve had two instances where people I had met several years ago who just asked me for advice on an idea, and I threw some significant cold water on their idea for legitimate reasons, I think, and legitimate reasons that they admitted too. They’re back. They’re back three years later, and they’ve adjusted, they’ve adapted, they’re still working on the same problem, but they’ve reinvented. Reinvented, if you will. They’ve adjusted. They’ve kept going. That willingness to persist is, I think, the biggest thing that is the biggest factor. It’s good news that people who go to spend a long time in school, who recognize that your final end point and final diploma granting point is many years away, they tend to be persistent people anyway. It’s a good cohort to be drawing from.

Matthew Maltese:          I think the second thing is, of course, don’t be hung up on your solution, because when you do that, you actually narrow the potential solutions to the problem. This is why, I think, separating needs finding and solution generation needs to be two separate things, because if you’re a hammer, everything looks like a nail. If you come in thinking that I’m going to solve this problem by a new type of stent, everything that you do for this particular problem will be a stent, when it could be something else completely different that actually solves the problem, that’s part of the stenting process, but maybe a just completely different solution.

Dan Henrich:     This sounds like something I’ve read in that Biodesign book you have on your desk there.

Matthew Maltese:          We keep it right at the hand, right at ready.

Dan Henrich:     We’ll have to put a link to that when we post this on our blog.

Matthew Maltese:          I would, I would. Biodesign is not rocket science, it really isn’t, but it’s a great book and a great framework that the group at Stanford has put together. It’s really critical to read it and read it fully and rethink how you approach medtech innovation through it.

Dan Henrich:     Let’s talk about a clinician innovator team, we’ll call it, they’ve gone through the initial steps of the process by that book. They have a clearly defined needs statement, and they have evaluated different solutions and settled on a particular pathway for good reason. We often at Smithwise, in our early interactions, we may deal with an innovator who has an idea and a patent or is working on filing their patent, and the model in their minds is, get a patent, get a prototype, and then Johnson & Johnson or some other really big device manufacturer is going to buy this from me, and that’s going to be my exit strategy. That’s almost never what we actually see.

Dan Henrich:     I guess particularly within the pediatric realm where there’s all these other challenges, as well, to gathering funding, what advice would you give to a team in that situation, that has what you would call a very legitimate solution to a very real problem, but there’s a long way to go before their device is going to be snapped up by a manufacturer?

Matthew Maltese:          First of all, I agree with your assessment. It often seems like the inventor may have a tendency to overvalue the idea, whereas the investor or the eventual acquirer, which may be one of these large device manufacturers, they value the proof. If you’re steeped in academia, this is the equivalent in academia. If you have a theory for how a particular disease mechanism, let’s say you have a theory, and you publish the theory. That’s basically worthless. It’s your idea, it’s your opinion. Not proven. It’s not until you take it into the laboratory or take it into the clinic or do some other empirical study to show, or not show, that your theory is right. A patent is like a theory, and it’s not a theory about whether the thing will work. It’s a theory about whether the market will accept it and buy it. It’s a theory as to whether your idea will add value to someone else’s life downstream. The second part of your question was?

Dan Henrich:     What advice would you, perhaps have you given, to a team that has a really good theory and really good evidence to suggest that it’s technically viable, they still need to attract investors, they still need to prove that value to the market? What advice would you give them?

Matthew Maltese:          I think, first of all, just recognize that, as I said earlier, the idea is just an idea. There are several stages that you can go through to increase the value of your idea. I don’t mean to say value in the sense of how much money it’s worth. That’s not what I mean. I mean in the sense of how viable is your product in making a difference in a patient’s life. The confidence, if you will, that X years from now, your idea will blossom into something that can make a difference.

Matthew Maltese:          If you have an idea and you’ve built a prototype and you’ve tried it out on a bench, on a phantom, or a surrogate for a human, you’ve proven the concept. Okay, so now you’ve notched up the likelihood a little bit that your idea will have some impact on somebody’s life downstream. Then, you figure out your regulatory pathway and you start down the pathway. By regulatory pathway, I mean, of course, what is the FDA going to want you to do before you can be cleared to sell the product? It’s an animal test, let’s say, or it’s a test on a human and so forth. Each one of these things is a milestone and is a risk reducer, if you will.

Matthew Maltese:          Then once you have your FDA clearance, you’re still not done, because you have to show to the potential acquirer that there is a market for the product. You have to go out and, in a very traditional door-to-door sort of way, sell it. Sell it. Then people who buy it may find that it has value or they may find that it doesn’t have value. The acquirer is looking for those initial indicators.

Matthew Maltese:          Now, there are no hard and fast rules as to when an acquirer will flip the switch and decide to take your device on and proliferate it across the world to benefit the lives of millions. It depends on the device, it depends on the idea. With some ideas and in some financial climates, something might be picked up very, very early in the process. In other climates or with other ideas, the acquirer is going to want more evidence. The short answer is, it depends. I’m sorry.

Dan Henrich:     No problem.

Matthew Maltese:          That’s reality, it depends.

Dan Henrich:     I think that’s a fitting piece of advice in this environment. If it were easy, it would be done by now. Matt, I really want to thank you for taking the time to talk with us about this. I think those of us who are within the industry really see a lot of promise for things changing and developing with regard to pediatric devices and helping underserved populations. I want to thank you for the role you’ve played in that and continue to play.

Matthew Maltese:          Thank you, Dan. Thank you for focusing on pediatrics. It is who is most important to us, and so I’m glad that you and Smithwise are making this part of who you are.

Dan Henrich:     It’s our pleasure. It’s been a good journey.

Matthew Maltese:          Thank you.

Written by Daniel Henrich

Written by Daniel Henrich

Director of Marketing at Archimedic