416 Episodo

  1. CDRH Proposed Guidance for FY 2023

    Publicado: 22/12/2022

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

    Publicado: 15/12/2022

  3. The Future of Healthcare & How We Get There

    Publicado: 8/12/2022

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

    Publicado: 30/11/2022

  5. Developing a Regulatory Strategy

    Publicado: 23/11/2022

  6. We Achieved ISO Certification! Now What?

    Publicado: 17/11/2022

  7. The Future of Reprocessed Used Medical Equipment

    Publicado: 11/11/2022

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

    Publicado: 4/11/2022

  9. Customer Discovery for Medical Device Companies

    Publicado: 2/11/2022

  10. EUA and the Impending Transition

    Publicado: 26/10/2022

  11. Common QMS Mistakes SaMD Companies Make

    Publicado: 21/10/2022

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

    Publicado: 13/10/2022

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

    Publicado: 6/10/2022

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

    Publicado: 29/9/2022

  15. Best Practices for Clinical Evidence Management

    Publicado: 22/9/2022

  16. Building Your Regulatory Strategy for Commercialization

    Publicado: 14/9/2022

  17. Packaging Validation Best Practices

    Publicado: 7/9/2022

  18. Overcoming Submission Deficiencies due to Biocompatibility

    Publicado: 1/9/2022

  19. Does Your CAPA Process Need a CAPA?

    Publicado: 24/8/2022

  20. UDI and the Current State of Global Implementation

    Publicado: 18/8/2022

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