Global Medical Device Podcast powered by Greenlight Guru

398 Folgen

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

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

   Vom: 12.3.2020
3. How to Choose the Right FDA Regulatory Pathway for your Device

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

   Vom: 19.2.2020
5. 4 Parts to Interviewing Candidates for Medical Device Roles

   Vom: 13.2.2020
6. 5 Tips for Hiring Medical Device Advisors

   Vom: 5.2.2020
7. 2 Key Areas Missing from FDA CDRH's Regulatory Science Priorities for 2020

   Vom: 29.1.2020
8. Navigating the Twists and Turns of Change Management for Medical Devices

   Vom: 28.12.2019
9. What is FDA's ASCA Pilot Program and How Does it Impact Medical Device Manufacturers?

   Vom: 19.12.2019
10. 5 Myths about QA/RA Recruiting in the Medical Device Industry

    Vom: 11.12.2019
11. How to Solve the Medtech Value Equation with Quality Data

    Vom: 5.12.2019
12. Why Supplier Quality Management Is So Important For Medical Device Companies

    Vom: 27.11.2019
13. Preparing for EU MDR

    Vom: 26.11.2019
14. FDA is Expanding its Case for Quality Program... Should Your Company Participate?

    Vom: 26.11.2019
15. Best Practices for Implementing Design Controls for the Medical Device Industry

    Vom: 7.11.2019
16. Should design controls have prevented the recent reprocessing tragedy: Do we need new regulation?

    Vom: 7.11.2019
17. How to Improve Your Medical Device Design Reviews Bonus Episode

    Vom: 7.11.2019
18. How To Improve Your Medical Device Design Reviews

    Vom: 7.11.2019
19. Risk Management from a Regulatory & Product Development Point of View

    Vom: 7.11.2019
20. How Proper Design Controls & a Quality System Could Save You $20M With Ronny Bracken

    Vom: 7.11.2019