Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. The Future of Cybersecurity

   Publisert: 30.4.2022
2. Achieving Operational Readiness through Good Project Management

   Publisert: 27.4.2022
3. Bridging the Gap between Medical Devices and Clinical Data

   Publisert: 20.4.2022
4. Navigating the Medical Device Single Audit Program (MDSAP)

   Publisert: 13.4.2022
5. Bringing Augmented Reality MedTech to Market

   Publisert: 7.4.2022
6. Making Your Informational Meetings with FDA Valuable & Worthwhile

   Publisert: 31.3.2022
7. Building Your Bill of Materials (BOM) to Accommodate Crossfunctional Needs

   Publisert: 23.3.2022
8. QMSR: The Future of FDA's Quality Management System Regulation for Medical Devices

   Publisert: 16.3.2022
9. How Medical Device Intellectual Property Protection Varies by Sector

   Publisert: 10.3.2022
10. Human Factors & Risk Management: What's Needed & Why?

    Publisert: 2.3.2022
11. What are the Opportunities for Improvement (OFI) for Quality?

    Publisert: 23.2.2022
12. Overcoming Barriers to Receiving 510(k) Clearance: One Company's Go-to-Market Triumph

    Publisert: 17.2.2022
13. How to Select a Contract Manufacturer

    Publisert: 2.2.2022
14. A Regulatory Gap Analysis of FDA's Systems & Policies

    Publisert: 27.1.2022
15. Greenlight Guru Acquires CanvasGT: A Fire(less)side Chat

    Publisert: 19.1.2022
16. Tips for Being Prepared Post-EUA (Emergency Use Authorization)

    Publisert: 13.1.2022
17. Understanding the UDI System for Medical Devices

    Publisert: 6.1.2022
18. Shaking Things Up: What's Next for the Global Medical Device Podcast

    Publisert: 16.12.2021
19. How Augmented Reality (AR) is Revolutionizing Healthcare

    Publisert: 9.12.2021
20. Why FDA is Prioritizing Clinical Decision Support Software & Why You Should Care

    Publisert: 2.12.2021