Global Medical Device Podcast powered by Greenlight Guru

416 Épisodes

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

   Publié: 26/02/2020
2. How to Establish a Solid Foundation for Fundraising and Product Success by Focusing on Regulatory

   Publié: 19/02/2020
3. 4 Parts to Interviewing Candidates for Medical Device Roles

   Publié: 13/02/2020
4. 5 Tips for Hiring Medical Device Advisors

   Publié: 05/02/2020
5. 2 Key Areas Missing from FDA CDRH's Regulatory Science Priorities for 2020

   Publié: 29/01/2020
6. Navigating the Twists and Turns of Change Management for Medical Devices

   Publié: 28/12/2019
7. What is FDA's ASCA Pilot Program and How Does it Impact Medical Device Manufacturers?

   Publié: 19/12/2019
8. 5 Myths about QA/RA Recruiting in the Medical Device Industry

   Publié: 11/12/2019
9. How to Solve the Medtech Value Equation with Quality Data

   Publié: 05/12/2019
10. Why Supplier Quality Management Is So Important For Medical Device Companies

    Publié: 27/11/2019
11. Preparing for EU MDR

    Publié: 26/11/2019
12. FDA is Expanding its Case for Quality Program... Should Your Company Participate?

    Publié: 26/11/2019
13. Helping Prepare Biomedical Engineers Entering the Workforce

    Publié: 07/11/2019
14. Tips, Tricks & Best Practices for Complying with ISO 13485:2016

    Publié: 07/11/2019
15. How to Ensure Your Quality Management System is Effective and Benefits Patients

    Publié: 07/11/2019
16. How to Use the Abbreviated FDA 510(k) Pathway to Your Advantage

    Publié: 07/11/2019
17. FDA Proposes Allowing Medical Device Makers to Summarize Malfunctions: What does that Mean for You?

    Publié: 07/11/2019
18. How to Design for Compliance with IEC 60601

    Publié: 07/11/2019
19. How to Think About Quality and Regulatory as Your Company Scales

    Publié: 07/11/2019
20. What are the Regulatory Expectations for Software as a Medical Device (SaMD)?

    Publié: 07/11/2019