Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

1. Bridging the Gap between Medical Devices and Clinical Data

   Gepubliceerd: 20-4-2022
2. Navigating the Medical Device Single Audit Program (MDSAP)

   Gepubliceerd: 13-4-2022
3. Bringing Augmented Reality MedTech to Market

   Gepubliceerd: 7-4-2022
4. Making Your Informational Meetings with FDA Valuable & Worthwhile

   Gepubliceerd: 30-3-2022
5. Building Your Bill of Materials (BOM) to Accommodate Crossfunctional Needs

   Gepubliceerd: 23-3-2022
6. QMSR: The Future of FDA's Quality Management System Regulation for Medical Devices

   Gepubliceerd: 16-3-2022
7. How Medical Device Intellectual Property Protection Varies by Sector

   Gepubliceerd: 9-3-2022
8. Human Factors & Risk Management: What's Needed & Why?

   Gepubliceerd: 2-3-2022
9. What are the Opportunities for Improvement (OFI) for Quality?

   Gepubliceerd: 23-2-2022
10. Overcoming Barriers to Receiving 510(k) Clearance: One Company's Go-to-Market Triumph

    Gepubliceerd: 17-2-2022
11. How to Select a Contract Manufacturer

    Gepubliceerd: 2-2-2022
12. A Regulatory Gap Analysis of FDA's Systems & Policies

    Gepubliceerd: 26-1-2022
13. Greenlight Guru Acquires CanvasGT: A Fire(less)side Chat

    Gepubliceerd: 19-1-2022
14. Tips for Being Prepared Post-EUA (Emergency Use Authorization)

    Gepubliceerd: 12-1-2022
15. Understanding the UDI System for Medical Devices

    Gepubliceerd: 6-1-2022
16. Shaking Things Up: What's Next for the Global Medical Device Podcast

    Gepubliceerd: 16-12-2021
17. How Augmented Reality (AR) is Revolutionizing Healthcare

    Gepubliceerd: 9-12-2021
18. Why FDA is Prioritizing Clinical Decision Support Software & Why You Should Care

    Gepubliceerd: 2-12-2021
19. Why Usability Matters

    Gepubliceerd: 24-11-2021
20. A Special Glimpse into Medtronic's Recent Developments in Spine & Biologics Technology

    Gepubliceerd: 17-11-2021