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. What is Regulatory Due Diligence for Medical Devices?

    Julkaistiin: 24.6.2020
  2. Mass-Manufacturing a 5-in-1 Ventilator System for COVID-19 Relief

    Julkaistiin: 18.6.2020
  3. How Being Strategic During A Career Transition Can Yield The Best Opportunities

    Julkaistiin: 11.6.2020
  4. Identifying the Positive and Negative Effects of COVID-19 on the Medical Device Industry

    Julkaistiin: 3.6.2020
  5. How to Construct an Effective Regulatory Strategy

    Julkaistiin: 27.5.2020
  6. What you Need to Know about Clinical Evaluation & Validation for Software as a Medical Device (SaMD)

    Julkaistiin: 21.5.2020
  7. How to Use Artificial Intelligence & Machine Learning to Produce Better, Smarter, Safer Devices

    Julkaistiin: 13.5.2020
  8. 510(k) Tips and Answers to Frequently Asked Questions for Medical Device Companies

    Julkaistiin: 6.5.2020
  9. Addressing the PPE Shortage with a No Cost Solution for Healthcare Providers

    Julkaistiin: 29.4.2020
  10. [LIVE] How EU MDR Changes are Impacting the Medical Device Ecosystem

    Julkaistiin: 22.4.2020
  11. How to Approach Verification and Validation for Cloud Software

    Julkaistiin: 15.4.2020
  12. Fighting COVID-19: How one MedTech Company is Using UV-C Technology to Eliminate Virus & Save Lives

    Julkaistiin: 10.4.2020
  13. Emergency Use Authorization (EUA) 101: What Medical Device Companies Need to Know

    Julkaistiin: 8.4.2020
  14. How to Integrate Usability into your Medical Device

    Julkaistiin: 1.4.2020
  15. [LIVE] Design Controls, Development & Risk for Software as a Medical Device (SaMD)

    Julkaistiin: 26.3.2020
  16. How to Leverage IEC 62304 to Improve SaMD Development Processes

    Julkaistiin: 18.3.2020
  17. What is the eSTAR Pilot Program and How Will it Improve FDA's 510(k) Review Process?

    Julkaistiin: 12.3.2020
  18. How to Choose the Right FDA Regulatory Pathway for your Device

    Julkaistiin: 26.2.2020
  19. How to Establish a Solid Foundation for Fundraising and Product Success by Focusing on Regulatory

    Julkaistiin: 19.2.2020
  20. 4 Parts to Interviewing Candidates for Medical Device Roles

    Julkaistiin: 13.2.2020

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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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