Global Medical Device Podcast powered by Greenlight Guru

398 Jaksot

1. Implementing Changes to SaMD under New EU MDR

   Julkaistiin: 7.11.2019
2. Leveraging Technology and Rapid Prototyping Methodologies during Product Development

   Julkaistiin: 7.11.2019
3. Is FDA's New 'Safer Technologies Program' Applicable To Your Medical Device?

   Julkaistiin: 7.11.2019
4. Understanding the Benefit-Risk Determinations of FDA's Latest Guidance Documents

   Julkaistiin: 7.11.2019
5. Addressing Top Questions of QA/RA Candidates on Salary, Skill Sets and Job Satisfaction

   Julkaistiin: 7.11.2019
6. 7 Habits of Highly Effective True Quality Medical Device Professionals

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

   Julkaistiin: 7.11.2019
8. Medical Device Industry Predictions for 2019

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

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

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

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

    Julkaistiin: 7.11.2019
13. Medical Device Product Development Value Proposition

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

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

    Julkaistiin: 7.11.2019
16. Who Should Own Your QMS?

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

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

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

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

    Julkaistiin: 7.11.2019