416 Episodes

  1. How Surgical Innovation Associates Found the Benefit of Quality Beyond Just Compliance

    Published: 11/7/2019
  2. Significant Risk vs. Nonsignificant Risk Devices - What's the Difference?

    Published: 11/7/2019
  3. How SimplicityMD Is Leveraging Technology to Help Get Their Devices to Market Faster

    Published: 11/7/2019
  4. How FDA Interacts with Medical Devices When They Are Imported into the US

    Published: 11/7/2019
  5. Understanding the Connection Between Complaints, CAPAs, and MDRs

    Published: 11/7/2019
  6. The Intersection of Medical Device Usability and Risk Management

    Published: 11/7/2019
  7. When Design Inputs Go Wrong + Design Your Label Like You Design Your Device

    Published: 11/7/2019
  8. Understanding FDA’s Proposed Conformity Assessment Pilot Program

    Published: 11/7/2019
  9. Understanding the Difference Between a General Wellness Device and a Regulated Medical Device

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

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

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

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

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

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

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

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

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

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

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

    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.