416 Épisodes

  1. #354: Advice for MedTech Regulatory Affairs Professionals

    Publié: 07/02/2024

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

    Publié: 30/01/2024

  3. #352: Fundamentals of Quality & Regulatory

    Publié: 18/01/2024

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

    Publié: 11/01/2024

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

    Publié: 04/01/2024

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

    Publié: 21/12/2023

  7. #348: Considerations for IVD

    Publié: 14/12/2023

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

    Publié: 07/12/2023

  9. #346: FDAs eSTAR Program

    Publié: 30/11/2023

  10. #345: Using AI In MedTech

    Publié: 22/11/2023

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

    Publié: 16/11/2023

  12. #343: Recent FDA Draft Guidances

    Publié: 09/11/2023

  13. #342: Planning an FDA Submission

    Publié: 02/11/2023

  14. #341: What NOT to say to FDA

    Publié: 25/10/2023

  15. #340: LDTs & the FDAs Proposed Ruling

    Publié: 19/10/2023

  16. #339: UDI and the State of EUDAMED

    Publié: 12/10/2023

  17. #338: Site Selection for Clinical Trials

    Publié: 06/10/2023

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

    Publié: 21/09/2023

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

    Publié: 14/09/2023

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

    Publié: 08/09/2023

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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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