Medtech Matters

Medical Product Outsourcing
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A podcast focused on the medical device technology industry, from design and development to outsourcing services and relationships to finished medtech products.

  1. 3 июн.

    Measuring Regulatory/Quality Team Member Performance

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re speaking about how to best determine the efficacy of regulatory and quality team members. A variety of real-world examples are provided that demonstrate the need to “trust but verify” the actions of these team members. During this conversation, the following questions are addressed: Why the need to measure the safety and efficacy of the regulatory and quality team?What can happen if you put too much trust or reliance on your regulatory consultant?Can you give a specific example where there was too much trust?Can you give us another regulatory example, perhaps involving clinical trials?Can you provide a quality or manufacturing example, perhaps involving AI?What are today’s takeaways?Listen to this discussion and see if you need a plan to verify your regulatory and quality team members’ actions. If you’d like to share thoughts, ask questions, or have a suggestion for a future topic for us to cover, please reach out to me at sfenske@rodmanmedia.com, and we’ll see if your ideas/inquiries/suggestions align with a future episode. Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    1 ч. 2 мин.

  2. 14 мая

    FDA's Third-Party Review Program

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re discussing the FDA’s third-party review program. This option is available for certain 510k reviews. It is performed through an independent organization that is not part of the agency. As such, there are additional costs involved but the time savings could potential make up for that added expense. Other factors and considerations are also reviewed. During this conversation, the following questions are addressed: If I need to get a 510k clearance on my new medical device, is going through the FDA my only option?Under what circumstances should a sponsor consider using the third-party review program?Under what circumstances should a sponsor not consider using the third-party review program?How popular is the third-party review program, i.e., why are many people not familiar with it?Can you provide some examples of devices that have gone through the third-party review program.What advice would you provide in choosing which third-party review organization to work with?What are the key steps when considering using the third-party review program?When evaluating potential third-party review organizations, do you have recommendations on what questions to ask?Is there anything like the third-party review program outside the US, i.e. is there any regulatory precedent?What else is important, and what are today’s takeaways?Listen to this discussion and see if you may have interest in the third-party review program. If you’d like to share thoughts, ask questions, or have a suggestion for a future topic for us to cover, please reach out to me at sfenske@rodmanmedia.com, and we’ll see if your ideas/inquiries/suggestions align with a future episode. Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    1 ч. 1 мин.

  3. 17 апр.

    Triaging Your QMS: Considerations Based on the New QMSR

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re discussing the FDA’s recently implemented QMSR. It went into effect on February 2nd and replaced 21 CFR Part 820. The regulation incorporates ISO 13485:2016, which is expected to help align medical device regulations globally. In this podcast, we focus on what device manufacturers should be doing now and what can wait for a later time. During this conversation, the following questions are addressed: As most are already familiar with QMS and now QMSR, we’ll dive deeper. Can you tell me if all sections of the QMSR listed in the QSR are required for all medical devices?Is a full QMS required to be in place in order to secure FDA clearance or approval?What about the sections of the QMSR? Are all of them equal in terms of importance? Are some sections more important than others?When do I need to have a QMS in place?What if I never intend to market my device? First, maybe provide an example of when that would be the case, and then address the first part.Should all QMS systems look the same?Are there differences with the QMSR with premarket vs. postmarket?How do you know the QMS is working? How can you be sure?What are the important takeaways from today’s session?Listen to this discussion and see if you are compliant with the new QMSR. If you’d like to share thoughts, ask questions, or have a suggestion for a future topic for us to cover, please reach out to me at sfenske@rodmanmedia.com, and we’ll see if your ideas/inquiries/suggestions align with a future episode. Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    59 мин.
  4. A Deep Dive into E&L and Biocomp Testing

    11 мар.

    A Deep Dive into E&L and Biocomp Testing

    In this Medtech Matters podcast episode, sponsored by Nelson Labs, we’re discussing the importance of E&L (extractables and leachables) and biocompatibility testing for a variety of medical devices. The pair from Nelson Labs—Audrey Turley, B.S., Director of Lab Operations – Biosafety, and Kristin Treece, Ph.D., Principal Scientist - Analytical Chemistry—bring their expertise to the conversation, where a number of issues are resolved. During this episode, the following questions are addressed: First, what is Nelson Labs? What do you do? What is E&L testing?Why is it important? What is being tested? Is this done on all medical devices?Are there different tests for E&L depending on the device and/or application?When is E&L testing performed?What is biocomp testing? Why is it important?When is it performed?How do you perform in vivo testing? (and what does in vivo mean?)Anything else device manufacturers need to know about E&L and/or biocomp testing?Listen to this discussion and see if you still have questions about E&L and/or biocompatibility testing. If you do, reach out to Nelson Labs to get answers. Feel free to use the links or contact mechanism here. Click here to learn more about Nelson Labs >>>>> Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    22 мин.

  5. 27.10.2025

    Planning for FDA Shutdowns Now and in the Future

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re discussing the government shutdown and its potential impact on medical device manufacturers and their submissions. This shutdown is almost one month in, and its conclusion does not seem to be in the near future. So, what do you do if you have a device being submitted to the FDA, already under review, or some other scenario involving the agency? During this conversation, the following questions are addressed: First, can you please explain what is out-of-bounds? (i.e., What will we NOT talk about?)What can FDA do during the shutdown?If a company currently has a submission under review, pending communications (e.g., emails, questions, pre-submission meetings), or other activities currently pending with the Agency, what would you advise the company to do? How should they proceed?If a company plans to make a submission, request a pre-submission meeting, or engage with FDA about other activities in the near future (but has not done so yet), what would you advise the company to do? How should they proceed?Can a company submit a pre-sub request during this shutdown?From a public policy perspective, how could situations like these be mitigated or possibly prevented in the future?What additional thoughts/questions/comments/concerns/recommendations/etc. do you think are important to share regarding the shutdown and its implications on medical device companies in particular and regulatory affairs in general?What else is important?What are today’s takeaways?Listen to this discussion and see if you can take action during the shutdown. If you’d like to share thoughts, ask questions, or have a suggestion for a future topic for us to cover, please reach out to me at sfenske@rodmanmedia.com and we’ll see if we want to address your ideas/inquiries/suggestions in a future episode. Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    57 мин.

  6. 11.09.2025

    Should Wellness Products Come with a Warning?

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re speaking about a recent Editor’s Letter I wrote for MPO that gave reasons why placing a warning label on wellness devices about their status as an FDA regulated medical device would be a good idea. Does Mike agree? Do you agree that patients should be provided with an explanation that a wellness product does not get reviewed or approved by the FDA? During this conversation, the following questions are addressed: My editorial is about wellness products. Before discussing further, can you remind us what a wellness product is?Why did you write this column and given wellness devices have been “formally recognized” by FDA since 2016, why did you write it now?In your title, you use Wellness Products vs. Wellness Devices. Why?You point out in your editorial that general wellness devices are low risk devices. In fact, that’s part of the title of the guidance. But is it correct to say, “General wellness devices are low-risk devices”?Let’s discuss the example from my editorial (SaltAir by Halosense).Should wellness devices be required to have a disclaimer regarding their lack of FDA review, or should it be the consumer's responsibility to research and find out more about the product on their own?If a disclaimer is recommended (maybe not required), what should the disclaimer say?What else is important?What are today’s takeaways?Listen to this discussion and see if you think wellness products should get a warning. If you’ Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    1 ч. 6 мин.

  7. 25.06.2025

    3 Most Common Premarket (Postmarket?) Review Issues FDA Sees

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re highlighting comments made by FDA representatives at an event about the most common premarket review issues they see in submissions. First, there is some discussion regarding whether the issues are truly premarket or postmarket concerns. Then, we look at what these are, why they are likely so common, examples of them, and how to avoid running into these issues yourself. During this conversation, the following questions are addressed: Recently, three medical device senior operations officers from FDA’s Office of Inspections and Investigations spoke at a conference about the most common “issues” FDA encounters during the premarketing review of medical devices. Can you give a recap of what they said?In your 30+ years of experience working in the medical device industry, would you agree with FDA that these are the three most common issues?Before discussing the three specific common problems individually, what do you think is the “root cause” of these problems?Can you provide some examples?How can design change and design creep get companies in trouble with FDA?What does “marketing beyond authorized intended use” mean?Do you have suggestions and/or best practices to avoid running into problems around these issues?What else is important?What are today’s takeaways?Listen to this discussion and see if you've run into these issues yourself. If you’d like to share thoughts, ask questions, or have a suggestion for a future topic for us to cover, please reach out to me at sfenske@rodmanmedia.com and Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    53 мин.

  8. 10.06.2025

    Why Are One-Third of MAUDE Reports a Problem?

    In this Medtech Matters podcast episode of Mike on Medtech with Mike Drues, president of Vascular Sciences, we’re discussing MAUDE safety reports and taking a look at what the issues are with them. More specifically, we’re digging in to find out why almost a third of the reports are delayed or incomplete. We’ll get insight on what these reports are, if they are important, and what should be done to improve that 30% figure. During this conversation, the following questions are addressed: First, Mike, if you would, please explain what the Manufacturer and User Facility Device Experience (MAUDE) Database is.What are the MAUDE reporting requirements?How well does the MAUDE reporting system work?Are there consequences for a delayed or incomplete report?Given the statistics, is the MAUDE database a reliable source of information for medical device manufactures? for clinicians? for patients? for anyone?What should manufacturers do?What should the FDA do?What else is important?What are today’s takeaways?Listen to this discussion and see if your company might have an issue with submitting a correct MAUDE report. If you’d like to share thoughts, ask questions, or have a suggestion for a future topic for us to cover, please reach out to me at sfenske@rodmanmedia.com and we’ll see if we want to address your ideas/inquiries/suggestions in a future episode. Send us Fan Mail For more medtech news and information, visit https://www.mpomag.com.

    58 мин.
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A podcast focused on the medical device technology industry, from design and development to outsourcing services and relationships to finished medtech products.

Информация

  • Автор
    Medical Product Outsourcing
  • Годы выхода
    2019 - 2026
  • Выпуски
    159
  • Ограничения
    С ненормативной лексикой
  • Авторские права
    © 2026 Medtech Matters
  • Сайт подкаста
    Medtech Matters

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