Global Medical Device Podcast powered by Greenlight Guru

416 Episoder

1. #354: Advice for MedTech Regulatory Affairs Professionals

   Publisert: 7.2.2024
2. #353: How Artificial Intelligence is Impacting the MedTech Industry

   Publisert: 30.1.2024
3. #352: Fundamentals of Quality & Regulatory

   Publisert: 18.1.2024
4. #351: The State of AI & Clinical Investigations

   Publisert: 11.1.2024
5. #350: The Evolving Landscape of AI in MedTech

   Publisert: 4.1.2024
6. #349: Climbing the MedTech Career Ladder - How to Get to the Top

   Publisert: 21.12.2023
7. #348: Considerations for IVD

   Publisert: 14.12.2023
8. #347: Human-Centered Design in Medical Devices

   Publisert: 7.12.2023
9. #346: FDAs eSTAR Program

   Publisert: 30.11.2023
10. #345: Using AI In MedTech

    Publisert: 22.11.2023
11. #344: Becoming an Advisor to a Medical Device Company

    Publisert: 16.11.2023
12. #343: Recent FDA Draft Guidances

    Publisert: 9.11.2023
13. #342: Planning an FDA Submission

    Publisert: 2.11.2023
14. #341: What NOT to say to FDA

    Publisert: 25.10.2023
15. #340: LDTs & the FDAs Proposed Ruling

    Publisert: 19.10.2023
16. #339: UDI and the State of EUDAMED

    Publisert: 12.10.2023
17. #338: Site Selection for Clinical Trials

    Publisert: 6.10.2023
18. #337: Moving MedTech Forward - The Past, Present & Future of Greenlight Guru

    Publisert: 21.9.2023
19. #336: From Academia to FDA Clearance (True Quality Roadshow - Boston)

    Publisert: 14.9.2023
20. #335: Accelerating SaMD Development in a Compliant Agile way

    Publisert: 8.9.2023