416 Avsnitt

  1. #354: Advice for MedTech Regulatory Affairs Professionals

    Publicerades: 2024-02-07

  2. #353: How Artificial Intelligence is Impacting the MedTech Industry

    Publicerades: 2024-01-30

  3. #352: Fundamentals of Quality & Regulatory

    Publicerades: 2024-01-18

  4. #351: The State of AI & Clinical Investigations

    Publicerades: 2024-01-11

  5. #350: The Evolving Landscape of AI in MedTech

    Publicerades: 2024-01-04

  6. #349: Climbing the MedTech Career Ladder - How to Get to the Top

    Publicerades: 2023-12-21

  7. #348: Considerations for IVD

    Publicerades: 2023-12-14

  8. #347: Human-Centered Design in Medical Devices

    Publicerades: 2023-12-07

  9. #346: FDAs eSTAR Program

    Publicerades: 2023-11-30

  10. #345: Using AI In MedTech

    Publicerades: 2023-11-22

  11. #344: Becoming an Advisor to a Medical Device Company

    Publicerades: 2023-11-16

  12. #343: Recent FDA Draft Guidances

    Publicerades: 2023-11-09

  13. #342: Planning an FDA Submission

    Publicerades: 2023-11-02

  14. #341: What NOT to say to FDA

    Publicerades: 2023-10-25

  15. #340: LDTs & the FDAs Proposed Ruling

    Publicerades: 2023-10-19

  16. #339: UDI and the State of EUDAMED

    Publicerades: 2023-10-12

  17. #338: Site Selection for Clinical Trials

    Publicerades: 2023-10-06

  18. #337: Moving MedTech Forward - The Past, Present & Future of Greenlight Guru

    Publicerades: 2023-09-21

  19. #336: From Academia to FDA Clearance (True Quality Roadshow - Boston)

    Publicerades: 2023-09-14

  20. #335: Accelerating SaMD Development in a Compliant Agile way

    Publicerades: 2023-09-08

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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.

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