416 Odcinki

  1. #354: Advice for MedTech Regulatory Affairs Professionals

    Opublikowany: 7.02.2024

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

    Opublikowany: 30.01.2024

  3. #352: Fundamentals of Quality & Regulatory

    Opublikowany: 18.01.2024

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

    Opublikowany: 11.01.2024

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

    Opublikowany: 4.01.2024

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

    Opublikowany: 21.12.2023

  7. #348: Considerations for IVD

    Opublikowany: 14.12.2023

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

    Opublikowany: 7.12.2023

  9. #346: FDAs eSTAR Program

    Opublikowany: 30.11.2023

  10. #345: Using AI In MedTech

    Opublikowany: 22.11.2023

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

    Opublikowany: 16.11.2023

  12. #343: Recent FDA Draft Guidances

    Opublikowany: 9.11.2023

  13. #342: Planning an FDA Submission

    Opublikowany: 2.11.2023

  14. #341: What NOT to say to FDA

    Opublikowany: 25.10.2023

  15. #340: LDTs & the FDAs Proposed Ruling

    Opublikowany: 19.10.2023

  16. #339: UDI and the State of EUDAMED

    Opublikowany: 12.10.2023

  17. #338: Site Selection for Clinical Trials

    Opublikowany: 6.10.2023

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

    Opublikowany: 21.09.2023

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

    Opublikowany: 14.09.2023

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

    Opublikowany: 8.09.2023

4 / 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