Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

1. Bridging the Gap between Medical Devices and Clinical Data

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

   Published: 4/13/2022
3. Bringing Augmented Reality MedTech to Market

   Published: 4/7/2022
4. Making Your Informational Meetings with FDA Valuable & Worthwhile

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

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

   Published: 3/16/2022
7. How Medical Device Intellectual Property Protection Varies by Sector

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

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

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

    Published: 2/17/2022
11. How to Select a Contract Manufacturer

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

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

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

    Published: 1/12/2022
15. Understanding the UDI System for Medical Devices

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

    Published: 12/16/2021
17. How Augmented Reality (AR) is Revolutionizing Healthcare

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

    Published: 12/2/2021
19. Why Usability Matters

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

    Published: 11/17/2021