Global Medical Device Podcast powered by Greenlight Guru

A podcast by Greenlight Guru + Medical Device Entrepreneurs - Thursdays

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398 Episodes

  1. Understanding the Difference Between a General Wellness Device and a Regulated Medical Device

    Published: 11/7/2019
  2. Why the 510(k) Process Is So Stressful & How You Can Help Streamline It

    Published: 11/7/2019
  3. How Competitive Regulatory Strategy Differs from Regular Regulatory Strategy

    Published: 11/7/2019
  4. How Process Excellence Leads to Product Excellence

    Published: 11/7/2019
  5. Comparing FDA Submission Types: 510(k) vs. De Novo vs. 513(g) vs. Pre-Submission

    Published: 11/7/2019
  6. Lessons to Be Learned From Recent FDA Inspections

    Published: 11/7/2019
  7. Understanding How to Use Real-World Evidence for Medical Device Regulatory Decisions

    Published: 11/7/2019
  8. Common Mistakes That Can Tank Your FDA 510(k) Submission

    Published: 11/7/2019
  9. An Overview of What Medical Device Developers Need to Know About Human Factors

    Published: 11/7/2019
  10. Challenges with Applying Risk Management Throughout the Manufacturing Process

    Published: 11/7/2019
  11. Evaluating FDA’s “New” Proposed Fast-Track Alternative Approach to the 510(k) Pathway

    Published: 11/7/2019
  12. What Substantial Equivalence Means as It Applies to 510(k)'s & Why It's So Important

    Published: 11/7/2019
  13. 5 Most Common Problems With Your CAPA Process

    Published: 11/7/2019
  14. How to Determine the Operational Quality of a Quality System Using a Performance Assessment

    Published: 11/7/2019
  15. Tips, Tricks & Best Practices for Complying with ISO 13485:2016

    Published: 11/7/2019
  16. Helping Prepare Biomedical Engineers Entering the Workforce

    Published: 11/7/2019
  17. How to Ensure Your Quality Management System is Effective and Benefits Patients

    Published: 11/7/2019
  18. Debunking Premarket Approval (PMA) Myths (And Why the PMA Path May Not Be as Scary as You Think)

    Published: 11/7/2019
  19. How to Think About Quality and Regulatory as Your Company Scales

    Published: 11/7/2019
  20. FDA Proposes Allowing Medical Device Makers to Summarize Malfunctions: What does that Mean for You?

    Published: 11/7/2019

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The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.