416 Odcinki

  1. How to Choose the Right FDA Regulatory Pathway for your Device

    Opublikowany: 26.02.2020

  2. How to Establish a Solid Foundation for Fundraising and Product Success by Focusing on Regulatory

    Opublikowany: 19.02.2020

  3. 4 Parts to Interviewing Candidates for Medical Device Roles

    Opublikowany: 13.02.2020

  4. 5 Tips for Hiring Medical Device Advisors

    Opublikowany: 5.02.2020

  5. 2 Key Areas Missing from FDA CDRH's Regulatory Science Priorities for 2020

    Opublikowany: 29.01.2020

  6. Navigating the Twists and Turns of Change Management for Medical Devices

    Opublikowany: 28.12.2019

  7. What is FDA's ASCA Pilot Program and How Does it Impact Medical Device Manufacturers?

    Opublikowany: 19.12.2019

  8. 5 Myths about QA/RA Recruiting in the Medical Device Industry

    Opublikowany: 11.12.2019

  9. How to Solve the Medtech Value Equation with Quality Data

    Opublikowany: 5.12.2019

  10. Why Supplier Quality Management Is So Important For Medical Device Companies

    Opublikowany: 27.11.2019

  11. Preparing for EU MDR

    Opublikowany: 26.11.2019

  12. FDA is Expanding its Case for Quality Program... Should Your Company Participate?

    Opublikowany: 26.11.2019

  13. Helping Prepare Biomedical Engineers Entering the Workforce

    Opublikowany: 7.11.2019

  14. Tips, Tricks & Best Practices for Complying with ISO 13485:2016

    Opublikowany: 7.11.2019

  15. How to Ensure Your Quality Management System is Effective and Benefits Patients

    Opublikowany: 7.11.2019

  16. How to Use the Abbreviated FDA 510(k) Pathway to Your Advantage

    Opublikowany: 7.11.2019

  17. FDA Proposes Allowing Medical Device Makers to Summarize Malfunctions: What does that Mean for You?

    Opublikowany: 7.11.2019

  18. How to Design for Compliance with IEC 60601

    Opublikowany: 7.11.2019

  19. How to Think About Quality and Regulatory as Your Company Scales

    Opublikowany: 7.11.2019

  20. What are the Regulatory Expectations for Software as a Medical Device (SaMD)?

    Opublikowany: 7.11.2019

15 / 21

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.

Visit the podcast's native language site