Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. #376: FDA's Proposed Wound Dressing Rule: Industry Impacts and Regulatory Insights

   Publisert: 18.7.2024
2. #375: Direct to Consumer - The Future of Healthcare

   Publisert: 11.7.2024
3. #374: Clinical Evidence - The Key to Market Adoption

   Publisert: 25.6.2024
4. #373: Creative Clinical Recruitment

   Publisert: 6.6.2024
5. #372: Getting Hired In MedTech

   Publisert: 4.6.2024
6. #370: Meet a Guru: Jamie Bihary

   Publisert: 30.5.2024
7. #371: Achieving ISO 13485 Certification

   Publisert: 28.5.2024
8. #369: Advice to Medical Device Inventors

   Publisert: 23.5.2024
9. #368: Institutional Review Boards (IRBs)

   Publisert: 21.5.2024
10. #367: Interviewing the Interviewer

    Publisert: 16.5.2024
11. #366: Cardiac Arrest: Five Heart-Stopping Years as a CEO on the Feds Hit-List

    Publisert: 9.5.2024
12. #365: Medical Device Reporting: The Do's and Don'ts

    Publisert: 7.5.2024
13. #363: Bringing a Self-Funded Medical Device to Market

    Publisert: 2.5.2024
14. #364: Building a Partnership with your Regulatory Consultant

    Publisert: 30.4.2024
15. #362: Managing Risk in Clinical Investigations

    Publisert: 25.4.2024
16. #361: Speaking the Language of IVD

    Publisert: 19.4.2024
17. #360: Is It Possible to "Buy" a QMS?

    Publisert: 11.4.2024
18. #359: Project Management in MedTech

    Publisert: 4.4.2024
19. #358: FDAs Voluntary Improvement Program

    Publisert: 21.3.2024
20. #357: The State of UDI Across the World

    Publisert: 7.3.2024