Global Medical Device Podcast powered by Greenlight Guru

416 Episoder

1. Meet a GURU: Jesseca Lyons

   Udgivet: 15.7.2020
2. How to Build a QMS for a Medical Device

   Udgivet: 8.7.2020
3. Meet a Guru: Taylor Brown

   Udgivet: 1.7.2020
4. What is Regulatory Due Diligence for Medical Devices?

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

   Udgivet: 17.6.2020
6. How Being Strategic During A Career Transition Can Yield The Best Opportunities

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

   Udgivet: 3.6.2020
8. How to Construct an Effective Regulatory Strategy

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

   Udgivet: 20.5.2020
10. How to Use Artificial Intelligence & Machine Learning to Produce Better, Smarter, Safer Devices

    Udgivet: 13.5.2020
11. 510(k) Tips and Answers to Frequently Asked Questions for Medical Device Companies

    Udgivet: 6.5.2020
12. Addressing the PPE Shortage with a No Cost Solution for Healthcare Providers

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

    Udgivet: 22.4.2020
14. How to Approach Verification and Validation for Cloud Software

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

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

    Udgivet: 8.4.2020
17. How to Integrate Usability into your Medical Device

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

    Udgivet: 26.3.2020
19. How to Leverage IEC 62304 to Improve SaMD Development Processes

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

    Udgivet: 12.3.2020