Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. Addressing Clinical Trial Challenges & Concerns during COVID-19

   Publisert: 29.7.2020
2. Protecting the Intellectual Property of your Medical Device Technology

   Publisert: 22.7.2020
3. Meet a GURU: Jesseca Lyons

   Publisert: 15.7.2020
4. How to Build a QMS for a Medical Device

   Publisert: 8.7.2020
5. Meet a Guru: Taylor Brown

   Publisert: 1.7.2020
6. What is Regulatory Due Diligence for Medical Devices?

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

   Publisert: 18.6.2020
8. How Being Strategic During A Career Transition Can Yield The Best Opportunities

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

   Publisert: 3.6.2020
10. How to Construct an Effective Regulatory Strategy

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

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

    Publisert: 13.5.2020
13. 510(k) Tips and Answers to Frequently Asked Questions for Medical Device Companies

    Publisert: 6.5.2020
14. Addressing the PPE Shortage with a No Cost Solution for Healthcare Providers

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

    Publisert: 22.4.2020
16. How to Approach Verification and Validation for Cloud Software

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

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

    Publisert: 8.4.2020
19. How to Integrate Usability into your Medical Device

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

    Publisert: 26.3.2020