416 Episoade

  1. CDRH Proposed Guidance for FY 2023

    Publicat: 22.12.2022

  2. Future of the Emergency Use Authorization (EUA): COVID, Monkeypox & Beyond

    Publicat: 15.12.2022

  3. The Future of Healthcare & How We Get There

    Publicat: 08.12.2022

  4. What "Exempt" Means with Respect to Medical Devices & Regulatory

    Publicat: 30.11.2022

  5. Developing a Regulatory Strategy

    Publicat: 23.11.2022

  6. We Achieved ISO Certification! Now What?

    Publicat: 17.11.2022

  7. The Future of Reprocessed Used Medical Equipment

    Publicat: 11.11.2022

  8. The Importance of Cervical Cancer Screening in the U.S.

    Publicat: 04.11.2022

  9. Customer Discovery for Medical Device Companies

    Publicat: 02.11.2022

  10. EUA and the Impending Transition

    Publicat: 26.10.2022

  11. Common QMS Mistakes SaMD Companies Make

    Publicat: 21.10.2022

  12. Design Assurance: The Unsung Heroes of R&D

    Publicat: 13.10.2022

  13. Lessons from an Industry Leader: Playing the Long Game of MedTech

    Publicat: 06.10.2022

  14. 7 Common 510(k) Mistakes and How to Avoid Them

    Publicat: 29.09.2022

  15. Best Practices for Clinical Evidence Management

    Publicat: 22.09.2022

  16. Building Your Regulatory Strategy for Commercialization

    Publicat: 14.09.2022

  17. Packaging Validation Best Practices

    Publicat: 07.09.2022

  18. Overcoming Submission Deficiencies due to Biocompatibility

    Publicat: 01.09.2022

  19. Does Your CAPA Process Need a CAPA?

    Publicat: 24.08.2022

  20. UDI and the Current State of Global Implementation

    Publicat: 18.08.2022

7 / 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