416 Épisodes

  1. CDRH Proposed Guidance for FY 2023

    Publié: 22/12/2022

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

    Publié: 15/12/2022

  3. The Future of Healthcare & How We Get There

    Publié: 08/12/2022

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

    Publié: 30/11/2022

  5. Developing a Regulatory Strategy

    Publié: 23/11/2022

  6. We Achieved ISO Certification! Now What?

    Publié: 17/11/2022

  7. The Future of Reprocessed Used Medical Equipment

    Publié: 11/11/2022

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

    Publié: 04/11/2022

  9. Customer Discovery for Medical Device Companies

    Publié: 02/11/2022

  10. EUA and the Impending Transition

    Publié: 26/10/2022

  11. Common QMS Mistakes SaMD Companies Make

    Publié: 21/10/2022

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

    Publié: 13/10/2022

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

    Publié: 06/10/2022

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

    Publié: 29/09/2022

  15. Best Practices for Clinical Evidence Management

    Publié: 22/09/2022

  16. Building Your Regulatory Strategy for Commercialization

    Publié: 14/09/2022

  17. Packaging Validation Best Practices

    Publié: 07/09/2022

  18. Overcoming Submission Deficiencies due to Biocompatibility

    Publié: 01/09/2022

  19. Does Your CAPA Process Need a CAPA?

    Publié: 24/08/2022

  20. UDI and the Current State of Global Implementation

    Publié: 18/08/2022

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