Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

1. CDRH Proposed Guidance for FY 2023

   Published: 12/22/2022
2. Future of the Emergency Use Authorization (EUA): COVID, Monkeypox & Beyond

   Published: 12/15/2022
3. The Future of Healthcare & How We Get There

   Published: 12/8/2022
4. What "Exempt" Means with Respect to Medical Devices & Regulatory

   Published: 11/30/2022
5. Developing a Regulatory Strategy

   Published: 11/23/2022
6. We Achieved ISO Certification! Now What?

   Published: 11/17/2022
7. The Future of Reprocessed Used Medical Equipment

   Published: 11/11/2022
8. The Importance of Cervical Cancer Screening in the U.S.

   Published: 11/4/2022
9. Customer Discovery for Medical Device Companies

   Published: 11/2/2022
10. EUA and the Impending Transition

    Published: 10/26/2022
11. Common QMS Mistakes SaMD Companies Make

    Published: 10/21/2022
12. Design Assurance: The Unsung Heroes of R&D

    Published: 10/13/2022
13. Lessons from an Industry Leader: Playing the Long Game of MedTech

    Published: 10/6/2022
14. 7 Common 510(k) Mistakes and How to Avoid Them

    Published: 9/29/2022
15. Best Practices for Clinical Evidence Management

    Published: 9/22/2022
16. Building Your Regulatory Strategy for Commercialization

    Published: 9/14/2022
17. Packaging Validation Best Practices

    Published: 9/7/2022
18. Overcoming Submission Deficiencies due to Biocompatibility

    Published: 9/1/2022
19. Does Your CAPA Process Need a CAPA?

    Published: 8/24/2022
20. UDI and the Current State of Global Implementation

    Published: 8/18/2022