Global Medical Device Podcast powered by Greenlight Guru

Podcast tekijän mukaan Greenlight Guru + Medical Device Entrepreneurs - Torstaisin

Torstaisin

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393 Jaksot

  1. Zebra Medical Technologies: How a New Breed of Medical Device Companies Is Leveraging Technology

    Julkaistiin: 7.11.2019
  2. Using the Bucket Method for Medical Device Risk Management w/ Mike Drues

    Julkaistiin: 7.11.2019
  3. Tips for Success When It Comes to IEC 60601 with Leo Eisner

    Julkaistiin: 7.11.2019
  4. 2016 Medical Device Regulatory Trends Year in Review

    Julkaistiin: 7.11.2019
  5. How Surgical Innovation Associates Found the Benefit of Quality Beyond Just Compliance

    Julkaistiin: 7.11.2019
  6. An Overview of What Device Makers Need to Know About CAPA

    Julkaistiin: 7.11.2019
  7. Significant Risk vs. Nonsignificant Risk Devices - What's the Difference?

    Julkaistiin: 7.11.2019
  8. How Phagenesis Is Using Regulatory Affairs as They Develop a Treatment for Dysphagia

    Julkaistiin: 7.11.2019
  9. What Devicemakers Need to Know About Medical Device Reporting (MDR)

    Julkaistiin: 7.11.2019
  10. How SimplicityMD Is Leveraging Technology to Help Get Their Devices to Market Faster

    Julkaistiin: 7.11.2019
  11. How FDA Interacts with Medical Devices When They Are Imported into the US

    Julkaistiin: 7.11.2019
  12. Understanding the Connection Between Complaints, CAPAs, and MDRs

    Julkaistiin: 7.11.2019
  13. The Intersection of Medical Device Usability and Risk Management

    Julkaistiin: 7.11.2019
  14. When Design Inputs Go Wrong + Design Your Label Like You Design Your Device

    Julkaistiin: 7.11.2019
  15. Understanding FDA’s Proposed Conformity Assessment Pilot Program

    Julkaistiin: 7.11.2019
  16. Understanding the Difference Between a General Wellness Device and a Regulated Medical Device

    Julkaistiin: 7.11.2019
  17. Why the 510(k) Process Is So Stressful & How You Can Help Streamline It

    Julkaistiin: 7.11.2019
  18. How Competitive Regulatory Strategy Differs from Regular Regulatory Strategy

    Julkaistiin: 7.11.2019
  19. Lessons to Be Learned From Recent FDA Inspections

    Julkaistiin: 7.11.2019
  20. How Process Excellence Leads to Product Excellence

    Julkaistiin: 7.11.2019

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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.

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