Global Medical Device Podcast powered by Greenlight Guru

393 Jaksot

1. 7 Habits of Highly Effective True Quality Medical Device Professionals

   Julkaistiin: 7.11.2019
2. Aligning True Quality and Compliance with MDDAP

   Julkaistiin: 7.11.2019
3. Understanding the Blurred Lines Between Consumer Tech and MedTech

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

   Julkaistiin: 7.11.2019
5. Medical Device Industry Predictions for 2019

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

   Julkaistiin: 7.11.2019
7. Why You Should Fear Product Liability Attorneys More Than Regulatory Agencies

   Julkaistiin: 7.11.2019
8. Medical Device Product Development Value Proposition

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

   Julkaistiin: 7.11.2019
10. Who Should Own Your QMS?

    Julkaistiin: 7.11.2019
11. Design Validation vs. Human Factors Validation

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

    Julkaistiin: 7.11.2019
13. How and When to Consider Human Factors

    Julkaistiin: 7.11.2019
14. Nonbinding Feedback is a New Guidance You Should Know About

    Julkaistiin: 7.11.2019
15. Grasping the Impact of Artificial Intelligence and Machine Learning on Medical Devices

    Julkaistiin: 7.11.2019
16. The 100th Episode: A Few of My Favorite Moments

    Julkaistiin: 7.11.2019
17. Live Atlanta True Quality Roadshow Panel: The Changing Quality & Regulatory Paradigm

    Julkaistiin: 7.11.2019
18. How to Make De Novo a Viable Option for your Medical Device

    Julkaistiin: 7.11.2019
19. Biocompatibility Nuances and its Impact on Medical Devices

    Julkaistiin: 7.11.2019
20. EU MDR: Not All Doom and Gloom

    Julkaistiin: 7.11.2019