Global Medical Device Podcast powered by Greenlight Guru

416 Odcinki

1. How to Determine the Operational Quality of a Quality System Using a Performance Assessment

   Opublikowany: 7.11.2019
2. 5 Most Common Problems With Your CAPA Process

   Opublikowany: 7.11.2019
3. Debunking Premarket Approval (PMA) Myths (And Why the PMA Path May Not Be as Scary as You Think)

   Opublikowany: 7.11.2019
4. 7 Habits of Highly Effective True Quality Medical Device Professionals

   Opublikowany: 7.11.2019
5. Aligning True Quality and Compliance with MDDAP

   Opublikowany: 7.11.2019
6. Explaining the Significance of Voluntary Consensus Standards

   Opublikowany: 7.11.2019
7. FDA Plans to Modernize 510(k) - Is the Sky Falling?

   Opublikowany: 7.11.2019
8. Medical Device Industry Predictions for 2019

   Opublikowany: 7.11.2019
9. Understanding the Blurred Lines Between Consumer Tech and MedTech

   Opublikowany: 7.11.2019
10. Quality Systems Management (QSM) vs. Quality Management System (QMS) - What's The Difference?

    Opublikowany: 7.11.2019
11. Medical Device Product Development Value Proposition

    Opublikowany: 7.11.2019
12. Why You Should Fear Product Liability Attorneys More Than Regulatory Agencies

    Opublikowany: 7.11.2019
13. Design Validation vs. Human Factors Validation

    Opublikowany: 7.11.2019
14. Who Should Own Your QMS?

    Opublikowany: 7.11.2019
15. Nonbinding Feedback is a New Guidance You Should Know About

    Opublikowany: 7.11.2019
16. Modernizing 510(k) Program through new FDA Safety and Performance Based Pathway

    Opublikowany: 7.11.2019
17. How and When to Consider Human Factors

    Opublikowany: 7.11.2019
18. Grasping the Impact of Artificial Intelligence and Machine Learning on Medical Devices

    Opublikowany: 7.11.2019
19. Live Atlanta True Quality Roadshow Panel: The Changing Quality & Regulatory Paradigm

    Opublikowany: 7.11.2019
20. The 100th Episode: A Few of My Favorite Moments

    Opublikowany: 7.11.2019