416 Épisodes

  1. #334: MedTech Funding and Preparing for Due Diligence

    Publié: 31/08/2023

  2. #333: Exploring Breakthrough Device Designation

    Publié: 25/08/2023

  3. #332: Regulatory Strategy and the Advantage of Diversity in MedTech

    Publié: 17/08/2023

  4. #331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues

    Publié: 10/08/2023

  5. #330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?

    Publié: 03/08/2023

  6. #329 The Right Way to Start a QMS: When, How, & What

    Publié: 27/07/2023

  7. #328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices

    Publié: 20/07/2023

  8. #327 Understanding the ROI of an eQMS

    Publié: 11/07/2023

  9. #326 CSA vs. CSV: Modern Validation for Modern MedTech

    Publié: 07/07/2023

  10. #325 The Role of dFMEAs in Risk Management for Medical Devices

    Publié: 30/06/2023

  11. #325 The Role of dFMEAs in Risk Management for Medical Devices

    Publié: 29/06/2023

  12. #324 Management Responsibility: The most important part of a QMS

    Publié: 22/06/2023

  13. #323 The Combination Products Handbook

    Publié: 16/06/2023

  14. Leaning into Lean Documentation

    Publié: 07/06/2023

  15. Cybersecurity and the Future of MedTech

    Publié: 02/06/2023

  16. How AI Can Help You Manage Risk

    Publié: 26/05/2023

  17. Ad Promo and The Difference in Regulatory & Legal

    Publié: 24/05/2023

  18. The Tools that Make Clinical Investigations

    Publié: 13/05/2023

  19. Complaint Handling with Medical Device Guru, Brittney McIver

    Publié: 03/05/2023

  20. Avoiding Potential Issues with your 510(k) Submission

    Publié: 27/04/2023

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The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.

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