Global Medical Device Podcast powered by Greenlight Guru

416 Episodio

1. CDRH Proposed Guidance for FY 2023

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

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

   Pubblicato: 08/12/2022
4. What "Exempt" Means with Respect to Medical Devices & Regulatory

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

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

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

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

   Pubblicato: 04/11/2022
9. Customer Discovery for Medical Device Companies

   Pubblicato: 02/11/2022
10. EUA and the Impending Transition

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

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

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

    Pubblicato: 06/10/2022
14. 7 Common 510(k) Mistakes and How to Avoid Them

    Pubblicato: 29/09/2022
15. Best Practices for Clinical Evidence Management

    Pubblicato: 22/09/2022
16. Building Your Regulatory Strategy for Commercialization

    Pubblicato: 14/09/2022
17. Packaging Validation Best Practices

    Pubblicato: 07/09/2022
18. Overcoming Submission Deficiencies due to Biocompatibility

    Pubblicato: 01/09/2022
19. Does Your CAPA Process Need a CAPA?

    Pubblicato: 24/08/2022
20. UDI and the Current State of Global Implementation

    Pubblicato: 18/08/2022