Global Medical Device Podcast powered by Greenlight Guru

398 Episodes

1. The Future of Cybersecurity

   Published: 4/30/2022
2. Achieving Operational Readiness through Good Project Management

   Published: 4/27/2022
3. Bridging the Gap between Medical Devices and Clinical Data

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

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

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

   Published: 3/31/2022
7. Building Your Bill of Materials (BOM) to Accommodate Crossfunctional Needs

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

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

   Published: 3/10/2022
10. Human Factors & Risk Management: What's Needed & Why?

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

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

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

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

    Published: 1/27/2022
15. Greenlight Guru Acquires CanvasGT: A Fire(less)side Chat

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

    Published: 1/13/2022
17. Understanding the UDI System for Medical Devices

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

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

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

    Published: 12/2/2021