416 Episodio

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

    Pubblicato: 07/11/2019

  2. Addressing Top Questions of QA/RA Candidates on Salary, Skill Sets and Job Satisfaction

    Pubblicato: 07/11/2019

  3. Best Practices for Implementing Design Controls for the Medical Device Industry

    Pubblicato: 07/11/2019

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

    Pubblicato: 07/11/2019

  5. How To Improve Your Medical Device Design Reviews

    Pubblicato: 07/11/2019

  6. How to Improve Your Medical Device Design Reviews Bonus Episode

    Pubblicato: 07/11/2019

  7. Risk Management from a Regulatory & Product Development Point of View

    Pubblicato: 07/11/2019

  8. Sara Naab On Going From Idea to Funding to One of the Bay Area's Most Innovative Life Sciences Co's

    Pubblicato: 07/11/2019

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

    Pubblicato: 07/11/2019

  10. How To Avoid Major Common Mistakes During the 510(k) Process with Michael Drues

    Pubblicato: 07/11/2019

  11. How To Identify, Quantify & Manage Enterprise Risks for Medical Device Companies with Mike Cremeans

    Pubblicato: 07/11/2019

  12. Tips, Tricks and Pointers for MedTech Startup Entrepreneurs With Mitch Levinson

    Pubblicato: 07/11/2019

  13. Why Medical Device Startups Need to Implement a ‘Right-Sized’ QMS with David Amor

    Pubblicato: 07/11/2019

  14. Why Design Inputs Are So Important to the Success or Failure of Your Project with Matt Romey

    Pubblicato: 07/11/2019

  15. An Insider’s Look at the Changes Coming in ISO 13485:2016 with Mark Swanson

    Pubblicato: 07/11/2019

  16. Why Using the Proper Standards for Your Regulatory Submission is So Important with Leo Eisner

    Pubblicato: 07/11/2019

  17. Medical Device Product Development Project Management Best Practices with Peter Sebelius

    Pubblicato: 07/11/2019

  18. The Difference Between Intended Use and Indications of Use with Mike Drues

    Pubblicato: 07/11/2019

  19. Why the Conventional Wisdom Regarding ‘R’ and ‘D’ in Medtech Product Development Is Wrong

    Pubblicato: 07/11/2019

  20. How to Avoid Medical Device Product Development Wipeouts with Meghan Alonso

    Pubblicato: 07/11/2019

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The Global Medical Device Podcast, powered by Greenlight Guru, is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.

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