Global Medical Device Podcast powered by Greenlight Guru

368 Episoder

1. #366: Cardiac Arrest: Five Heart-Stopping Years as a CEO on the Feds Hit-List

   Publisert: 9.5.2024
2. #365: Medical Device Reporting: The Do's and Don'ts

   Publisert: 2.5.2024
3. #364: Building a Partnership with your Regulatory Consultant

   Publisert: 30.4.2024
4. #363: Bringing a Self-Funded Medical Device to Market

   Publisert: 25.4.2024
5. #362: Managing Risk in Clinical Investigations

   Publisert: 23.4.2024
6. #361: Speaking the Language of IVD

   Publisert: 19.4.2024
7. #360: Is It Possible to "Buy" a QMS?

   Publisert: 13.4.2024
8. #359: Project Management in MedTech

   Publisert: 4.4.2024
9. #358: FDAs Voluntary Improvement Program

   Publisert: 21.3.2024
10. #357: The State of UDI Across the World

    Publisert: 7.3.2024
11. #356: Quality Myths & Lessons Learned Part II

    Publisert: 22.2.2024
12. #355: Mastering the Pitch: MedTech Innovations from Concept to Market

    Publisert: 15.2.2024
13. #354: Advice for MedTech Regulatory Affairs Professionals

    Publisert: 7.2.2024
14. #353: How Artificial Intelligence is Impacting the MedTech Industry

    Publisert: 30.1.2024
15. #352: Fundamentals of Quality & Regulatory

    Publisert: 18.1.2024
16. #351: The State of AI & Clinical Investigations

    Publisert: 11.1.2024
17. #350: The Evolving Landscape of AI in MedTech

    Publisert: 4.1.2024
18. #349: Climbing the MedTech Career Ladder - How to Get to the Top

    Publisert: 21.12.2023
19. #348: Considerations for IVD

    Publisert: 14.12.2023
20. #347: Human-Centered Design in Medical Devices

    Publisert: 7.12.2023