416 Episodes

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

    Published: 7/7/2025
  2. #413: Budgeting Blind Spots: What MedTech Startups Miss—and How Investors See It

    Published: 6/30/2025
  3. #412: How to Build a QMS That Actually Works: From Startup to Scale in MedTech

    Published: 6/23/2025
  4. #411: Unlocking U.S. MedTech Market Access: State-Specific Compliance Pitfalls Medical Device Companies Miss

    Published: 6/16/2025
  5. #410: Is the MAUDE Database Broken? An Insider’s Take on Adverse Event Reporting Failures

    Published: 6/9/2025
  6. #409: How Iterative Management Transforms MedTech Teams: Faster Execution, Smarter Decisions

    Published: 6/2/2025
  7. #408: What MedTech Startups Miss: Design Mistakes, Risk Testing & the Myth of the Quick Exit

    Published: 5/26/2025
  8. #407: Cybersecurity in MedTech: FDA Compliance, Patient Safety & the Hidden Risks You’re Missing

    Published: 5/19/2025
  9. #406: Over the Counter (OTC) vs. Prescription (RX) Medical Devices, Pt. 2

    Published: 5/12/2025
  10. #405: Over the Counter (OTC) vs. Prescription (RX) Medical Devices, Pt. 1

    Published: 5/5/2025
  11. #404: MedTech 101: What You Need to Know About the Medical Device Industry

    Published: 5/1/2025
  12. #403: Global Perspective on Medical Device Reimbursement

    Published: 4/24/2025
  13. #402: How to Attract Real Talent in the Medical Device Industry

    Published: 4/17/2025
  14. #401: FDA’s Vital Role in ISO Standards: Ensuring Global MedTech Integrity

    Published: 4/10/2025
  15. #400: The State of the Medical Device Industry

    Published: 4/3/2025
  16. #399: How To Approach Culture Differences

    Published: 2/20/2025
  17. #398: Game-Changing Connections in MedTech: Inside LSI with Scott Pantel

    Published: 2/13/2025
  18. #397: Winning Over Skeptics: the Key to Product Adoption in Healthcare

    Published: 2/6/2025
  19. #396: Mastering Device Descriptions: The Cornerstone of Medical Device Submissions

    Published: 12/19/2024
  20. #395: IEC 60601 Updates: What MedTech Professionals Need to Know for 2025 and Beyond

    Published: 12/12/2024

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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.