Global Medical Device Podcast powered by Greenlight Guru

416 Episodo

1. Meet a GURU: Jesseca Lyons

   Publicado: 15/7/2020
2. How to Build a QMS for a Medical Device

   Publicado: 8/7/2020
3. Meet a Guru: Taylor Brown

   Publicado: 1/7/2020
4. What is Regulatory Due Diligence for Medical Devices?

   Publicado: 24/6/2020
5. Mass-Manufacturing a 5-in-1 Ventilator System for COVID-19 Relief

   Publicado: 17/6/2020
6. How Being Strategic During A Career Transition Can Yield The Best Opportunities

   Publicado: 11/6/2020
7. Identifying the Positive and Negative Effects of COVID-19 on the Medical Device Industry

   Publicado: 3/6/2020
8. How to Construct an Effective Regulatory Strategy

   Publicado: 27/5/2020
9. What you Need to Know about Clinical Evaluation & Validation for Software as a Medical Device (SaMD)

   Publicado: 20/5/2020
10. How to Use Artificial Intelligence & Machine Learning to Produce Better, Smarter, Safer Devices

    Publicado: 13/5/2020
11. 510(k) Tips and Answers to Frequently Asked Questions for Medical Device Companies

    Publicado: 6/5/2020
12. Addressing the PPE Shortage with a No Cost Solution for Healthcare Providers

    Publicado: 29/4/2020
13. [LIVE] How EU MDR Changes are Impacting the Medical Device Ecosystem

    Publicado: 22/4/2020
14. How to Approach Verification and Validation for Cloud Software

    Publicado: 15/4/2020
15. Fighting COVID-19: How one MedTech Company is Using UV-C Technology to Eliminate Virus & Save Lives

    Publicado: 10/4/2020
16. Emergency Use Authorization (EUA) 101: What Medical Device Companies Need to Know

    Publicado: 8/4/2020
17. How to Integrate Usability into your Medical Device

    Publicado: 1/4/2020
18. [LIVE] Design Controls, Development & Risk for Software as a Medical Device (SaMD)

    Publicado: 26/3/2020
19. How to Leverage IEC 62304 to Improve SaMD Development Processes

    Publicado: 18/3/2020
20. What is the eSTAR Pilot Program and How Will it Improve FDA's 510(k) Review Process?

    Publicado: 12/3/2020