Global Medical Device Podcast powered by Greenlight Guru

368 Episodes

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

   Published: 5/9/2024
2. #365: Medical Device Reporting: The Do's and Don'ts

   Published: 5/2/2024
3. #364: Building a Partnership with your Regulatory Consultant

   Published: 4/30/2024
4. #363: Bringing a Self-Funded Medical Device to Market

   Published: 4/25/2024
5. #362: Managing Risk in Clinical Investigations

   Published: 4/23/2024
6. #361: Speaking the Language of IVD

   Published: 4/19/2024
7. #360: Is It Possible to "Buy" a QMS?

   Published: 4/13/2024
8. #359: Project Management in MedTech

   Published: 4/4/2024
9. #358: FDAs Voluntary Improvement Program

   Published: 3/21/2024
10. #357: The State of UDI Across the World

    Published: 3/7/2024
11. #356: Quality Myths & Lessons Learned Part II

    Published: 2/22/2024
12. #355: Mastering the Pitch: MedTech Innovations from Concept to Market

    Published: 2/15/2024
13. #354: Advice for MedTech Regulatory Affairs Professionals

    Published: 2/7/2024
14. #353: How Artificial Intelligence is Impacting the MedTech Industry

    Published: 1/30/2024
15. #352: Fundamentals of Quality & Regulatory

    Published: 1/18/2024
16. #351: The State of AI & Clinical Investigations

    Published: 1/11/2024
17. #350: The Evolving Landscape of AI in MedTech

    Published: 1/4/2024
18. #349: Climbing the MedTech Career Ladder - How to Get to the Top

    Published: 12/21/2023
19. #348: Considerations for IVD

    Published: 12/14/2023
20. #347: Human-Centered Design in Medical Devices

    Published: 12/7/2023