416 Épisodes

  1. #414: Why Global Certification is the Future of Clinical Research in Latin America

    Publié: 07/07/2025

  2. #413: Budgeting Blind Spots: What MedTech Startups Miss—and How Investors See It

    Publié: 30/06/2025

  3. #412: How to Build a QMS That Actually Works: From Startup to Scale in MedTech

    Publié: 23/06/2025

  4. #411: Unlocking U.S. MedTech Market Access: State-Specific Compliance Pitfalls Medical Device Companies Miss

    Publié: 16/06/2025

  5. #410: Is the MAUDE Database Broken? An Insider’s Take on Adverse Event Reporting Failures

    Publié: 09/06/2025

  6. #409: How Iterative Management Transforms MedTech Teams: Faster Execution, Smarter Decisions

    Publié: 02/06/2025

  7. #408: What MedTech Startups Miss: Design Mistakes, Risk Testing & the Myth of the Quick Exit

    Publié: 26/05/2025

  8. #407: Cybersecurity in MedTech: FDA Compliance, Patient Safety & the Hidden Risks You’re Missing

    Publié: 19/05/2025

  9. #406: Over the Counter (OTC) vs. Prescription (RX) Medical Devices, Pt. 2

    Publié: 12/05/2025

  10. #405: Over the Counter (OTC) vs. Prescription (RX) Medical Devices, Pt. 1

    Publié: 05/05/2025

  11. #404: MedTech 101: What You Need to Know About the Medical Device Industry

    Publié: 01/05/2025

  12. #403: Global Perspective on Medical Device Reimbursement

    Publié: 24/04/2025

  13. #402: How to Attract Real Talent in the Medical Device Industry

    Publié: 17/04/2025

  14. #401: FDA’s Vital Role in ISO Standards: Ensuring Global MedTech Integrity

    Publié: 10/04/2025

  15. #400: The State of the Medical Device Industry

    Publié: 03/04/2025

  16. #399: How To Approach Culture Differences

    Publié: 20/02/2025

  17. #398: Game-Changing Connections in MedTech: Inside LSI with Scott Pantel

    Publié: 13/02/2025

  18. #397: Winning Over Skeptics: the Key to Product Adoption in Healthcare

    Publié: 06/02/2025

  19. #396: Mastering Device Descriptions: The Cornerstone of Medical Device Submissions

    Publié: 19/12/2024

  20. #395: IEC 60601 Updates: What MedTech Professionals Need to Know for 2025 and Beyond

    Publié: 12/12/2024

1 / 21

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.

Visit the podcast's native language site