Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

1. Is FDA's New 'Safer Technologies Program' Applicable To Your Medical Device?

   Gepubliceerd: 7-11-2019
2. Addressing Top Questions of QA/RA Candidates on Salary, Skill Sets and Job Satisfaction

   Gepubliceerd: 7-11-2019
3. Best Practices for Implementing Design Controls for the Medical Device Industry

   Gepubliceerd: 7-11-2019
4. Should design controls have prevented the recent reprocessing tragedy: Do we need new regulation?

   Gepubliceerd: 7-11-2019
5. How To Improve Your Medical Device Design Reviews

   Gepubliceerd: 7-11-2019
6. How to Improve Your Medical Device Design Reviews Bonus Episode

   Gepubliceerd: 7-11-2019
7. Risk Management from a Regulatory & Product Development Point of View

   Gepubliceerd: 7-11-2019
8. Sara Naab On Going From Idea to Funding to One of the Bay Area's Most Innovative Life Sciences Co's

   Gepubliceerd: 7-11-2019
9. How Proper Design Controls & a Quality System Could Save You $20M With Ronny Bracken

   Gepubliceerd: 7-11-2019
10. How To Avoid Major Common Mistakes During the 510(k) Process with Michael Drues

    Gepubliceerd: 7-11-2019
11. How To Identify, Quantify & Manage Enterprise Risks for Medical Device Companies with Mike Cremeans

    Gepubliceerd: 7-11-2019
12. Tips, Tricks and Pointers for MedTech Startup Entrepreneurs With Mitch Levinson

    Gepubliceerd: 7-11-2019
13. Why Medical Device Startups Need to Implement a ‘Right-Sized’ QMS with David Amor

    Gepubliceerd: 7-11-2019
14. Why Design Inputs Are So Important to the Success or Failure of Your Project with Matt Romey

    Gepubliceerd: 7-11-2019
15. An Insider’s Look at the Changes Coming in ISO 13485:2016 with Mark Swanson

    Gepubliceerd: 7-11-2019
16. Why Using the Proper Standards for Your Regulatory Submission is So Important with Leo Eisner

    Gepubliceerd: 7-11-2019
17. Medical Device Product Development Project Management Best Practices with Peter Sebelius

    Gepubliceerd: 7-11-2019
18. The Difference Between Intended Use and Indications of Use with Mike Drues

    Gepubliceerd: 7-11-2019
19. Why the Conventional Wisdom Regarding ‘R’ and ‘D’ in Medtech Product Development Is Wrong

    Gepubliceerd: 7-11-2019
20. How to Avoid Medical Device Product Development Wipeouts with Meghan Alonso

    Gepubliceerd: 7-11-2019