Global Medical Device Podcast powered by Greenlight Guru

360 Episodes

1. #358: FDAs Voluntary Improvement Program

   Published: 3/21/2024
2. #357: The State of UDI Across the World

   Published: 3/7/2024
3. #356: Quality Myths & Lessons Learned Part II

   Published: 2/22/2024
4. #355: Mastering the Pitch: MedTech Innovations from Concept to Market

   Published: 2/15/2024
5. #354: Becoming a MedTech Regulatory Affairs Professional

   Published: 2/7/2024
6. #353: How Artificial Intelligence is Impacting the MedTech Industry

   Published: 1/30/2024
7. #352: Fundamentals of Quality & Regulatory

   Published: 1/18/2024
8. #351: The State of AI & Clinical Investigations

   Published: 1/11/2024
9. #350: The Evolving Landscape of AI in MedTech

   Published: 1/4/2024
10. #349: Climbing the MedTech Career Ladder - How to Get to the Top

    Published: 12/21/2023
11. #348: Considerations for IVD

    Published: 12/14/2023
12. #347: Human-Centered Design in Medical Devices

    Published: 12/7/2023
13. #346: FDAs eSTAR Program

    Published: 11/30/2023
14. #345: Using AI In MedTech

    Published: 11/22/2023
15. #344: Becoming an Advisor to a Medical Device Company

    Published: 11/16/2023
16. #343: Recent FDA Draft Guidances

    Published: 11/9/2023
17. #342: Planning an FDA Submission

    Published: 11/2/2023
18. #341: What NOT to say to FDA

    Published: 10/25/2023
19. #340: LDTs & the FDAs Proposed Ruling

    Published: 10/19/2023
20. #339: UDI and the State of EUDAMED

    Published: 10/12/2023