416 Afleveringen

  1. Meet a GURU: Jesseca Lyons

    Gepubliceerd: 15-7-2020

  2. How to Build a QMS for a Medical Device

    Gepubliceerd: 8-7-2020

  3. Meet a Guru: Taylor Brown

    Gepubliceerd: 1-7-2020

  4. What is Regulatory Due Diligence for Medical Devices?

    Gepubliceerd: 24-6-2020

  5. Mass-Manufacturing a 5-in-1 Ventilator System for COVID-19 Relief

    Gepubliceerd: 17-6-2020

  6. How Being Strategic During A Career Transition Can Yield The Best Opportunities

    Gepubliceerd: 11-6-2020

  7. Identifying the Positive and Negative Effects of COVID-19 on the Medical Device Industry

    Gepubliceerd: 3-6-2020

  8. How to Construct an Effective Regulatory Strategy

    Gepubliceerd: 27-5-2020

  9. What you Need to Know about Clinical Evaluation & Validation for Software as a Medical Device (SaMD)

    Gepubliceerd: 20-5-2020

  10. How to Use Artificial Intelligence & Machine Learning to Produce Better, Smarter, Safer Devices

    Gepubliceerd: 13-5-2020

  11. 510(k) Tips and Answers to Frequently Asked Questions for Medical Device Companies

    Gepubliceerd: 6-5-2020

  12. Addressing the PPE Shortage with a No Cost Solution for Healthcare Providers

    Gepubliceerd: 29-4-2020

  13. [LIVE] How EU MDR Changes are Impacting the Medical Device Ecosystem

    Gepubliceerd: 22-4-2020

  14. How to Approach Verification and Validation for Cloud Software

    Gepubliceerd: 15-4-2020

  15. Fighting COVID-19: How one MedTech Company is Using UV-C Technology to Eliminate Virus & Save Lives

    Gepubliceerd: 10-4-2020

  16. Emergency Use Authorization (EUA) 101: What Medical Device Companies Need to Know

    Gepubliceerd: 8-4-2020

  17. How to Integrate Usability into your Medical Device

    Gepubliceerd: 1-4-2020

  18. [LIVE] Design Controls, Development & Risk for Software as a Medical Device (SaMD)

    Gepubliceerd: 26-3-2020

  19. How to Leverage IEC 62304 to Improve SaMD Development Processes

    Gepubliceerd: 18-3-2020

  20. What is the eSTAR Pilot Program and How Will it Improve FDA's 510(k) Review Process?

    Gepubliceerd: 12-3-2020

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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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