Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. What is MedTech Lifecycle Excellence?

   Publisert: 5.1.2023
2. The Best of Jon & Mike Through the Years

   Publisert: 29.12.2022
3. CDRH Proposed Guidance for FY 2023

   Publisert: 22.12.2022
4. Future of the Emergency Use Authorization (EUA): COVID, Monkeypox & Beyond

   Publisert: 15.12.2022
5. The Future of Healthcare & How We Get There

   Publisert: 8.12.2022
6. What "Exempt" Means with Respect to Medical Devices & Regulatory

   Publisert: 30.11.2022
7. Developing a Regulatory Strategy

   Publisert: 23.11.2022
8. We Achieved ISO Certification! Now What?

   Publisert: 17.11.2022
9. The Future of Reprocessed Used Medical Equipment

   Publisert: 11.11.2022
10. The Importance of Cervical Cancer Screening in the U.S.

    Publisert: 4.11.2022
11. Customer Discovery for Medical Device Companies

    Publisert: 2.11.2022
12. EUA and the Impending Transition

    Publisert: 26.10.2022
13. Common QMS Mistakes SaMD Companies Make

    Publisert: 21.10.2022
14. Design Assurance: The Unsung Heroes of R&D

    Publisert: 13.10.2022
15. Lessons from an Industry Leader: Playing the Long Game of MedTech

    Publisert: 6.10.2022
16. 7 Common 510(k) Mistakes and How to Avoid Them

    Publisert: 29.9.2022
17. Best Practices for Clinical Evidence Management

    Publisert: 22.9.2022
18. Building Your Regulatory Strategy for Commercialization

    Publisert: 14.9.2022
19. Packaging Validation Best Practices

    Publisert: 8.9.2022
20. Overcoming Submission Deficiencies due to Biocompatibility

    Publisert: 1.9.2022