Global Medical Device Podcast powered by Greenlight Guru

416 Episoade

1. Bridging the Gap between Medical Devices and Clinical Data

   Publicat: 20.04.2022
2. Navigating the Medical Device Single Audit Program (MDSAP)

   Publicat: 13.04.2022
3. Bringing Augmented Reality MedTech to Market

   Publicat: 07.04.2022
4. Making Your Informational Meetings with FDA Valuable & Worthwhile

   Publicat: 30.03.2022
5. Building Your Bill of Materials (BOM) to Accommodate Crossfunctional Needs

   Publicat: 23.03.2022
6. QMSR: The Future of FDA's Quality Management System Regulation for Medical Devices

   Publicat: 16.03.2022
7. How Medical Device Intellectual Property Protection Varies by Sector

   Publicat: 09.03.2022
8. Human Factors & Risk Management: What's Needed & Why?

   Publicat: 02.03.2022
9. What are the Opportunities for Improvement (OFI) for Quality?

   Publicat: 23.02.2022
10. Overcoming Barriers to Receiving 510(k) Clearance: One Company's Go-to-Market Triumph

    Publicat: 17.02.2022
11. How to Select a Contract Manufacturer

    Publicat: 02.02.2022
12. A Regulatory Gap Analysis of FDA's Systems & Policies

    Publicat: 26.01.2022
13. Greenlight Guru Acquires CanvasGT: A Fire(less)side Chat

    Publicat: 19.01.2022
14. Tips for Being Prepared Post-EUA (Emergency Use Authorization)

    Publicat: 12.01.2022
15. Understanding the UDI System for Medical Devices

    Publicat: 06.01.2022
16. Shaking Things Up: What's Next for the Global Medical Device Podcast

    Publicat: 16.12.2021
17. How Augmented Reality (AR) is Revolutionizing Healthcare

    Publicat: 09.12.2021
18. Why FDA is Prioritizing Clinical Decision Support Software & Why You Should Care

    Publicat: 02.12.2021
19. Why Usability Matters

    Publicat: 24.11.2021
20. A Special Glimpse into Medtronic's Recent Developments in Spine & Biologics Technology

    Publicat: 17.11.2021