Global Medical Device Podcast powered by Greenlight Guru

393 Jaksot

1. Making Your Informational Meetings with FDA Valuable & Worthwhile

   Julkaistiin: 31.3.2022
2. Building Your Bill of Materials (BOM) to Accommodate Crossfunctional Needs

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

   Julkaistiin: 16.3.2022
4. How Medical Device Intellectual Property Protection Varies by Sector

   Julkaistiin: 10.3.2022
5. Human Factors & Risk Management: What's Needed & Why?

   Julkaistiin: 2.3.2022
6. What are the Opportunities for Improvement (OFI) for Quality?

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

   Julkaistiin: 17.2.2022
8. How to Select a Contract Manufacturer

   Julkaistiin: 2.2.2022
9. A Regulatory Gap Analysis of FDA's Systems & Policies

   Julkaistiin: 27.1.2022
10. Greenlight Guru Acquires CanvasGT: A Fire(less)side Chat

    Julkaistiin: 19.1.2022
11. Tips for Being Prepared Post-EUA (Emergency Use Authorization)

    Julkaistiin: 13.1.2022
12. Understanding the UDI System for Medical Devices

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

    Julkaistiin: 16.12.2021
14. How Augmented Reality (AR) is Revolutionizing Healthcare

    Julkaistiin: 9.12.2021
15. Why FDA is Prioritizing Clinical Decision Support Software & Why You Should Care

    Julkaistiin: 2.12.2021
16. Why Usability Matters

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

    Julkaistiin: 18.11.2021
18. What are the Top Compliance Issues Plaguing Medical Device Manufacturers?

    Julkaistiin: 10.11.2021
19. Setting the Record Straight on Usability & Human Factors

    Julkaistiin: 3.11.2021
20. Project Management for Product Development of Medical Devices

    Julkaistiin: 27.10.2021