Global Medical Device Podcast powered by Greenlight Guru

398 Episoder

1. How to Design for Compliance with IEC 60601

   Publisert: 7.11.2019
2. How to Use the Abbreviated FDA 510(k) Pathway to Your Advantage

   Publisert: 7.11.2019
3. How Human Factors Impact Your Medical Device

   Publisert: 7.11.2019
4. What you Need to Know about FDA's Progressive Programs

   Publisert: 7.11.2019
5. What are the Regulatory Expectations for Software as a Medical Device (SaMD)?

   Publisert: 7.11.2019
6. The Bleeding Edge: Lessons Learned for the Medical Device Industry

   Publisert: 7.11.2019
7. AI Explainability: What that Means and Why it Matters in the Medical Device Industry

   Publisert: 7.11.2019
8. 15 Habits of Highly Effective Regulatory Professionals

   Publisert: 7.11.2019
9. Regulatory Tips & Observations from a Former FDA Reviewer

   Publisert: 7.11.2019
10. What You Need to Know About The FDA CDRH Experiential Learning Program

    Publisert: 7.11.2019
11. Questions to Ask Before Hiring Your QA/RA Consultant

    Publisert: 7.11.2019
12. Latest Updates on CDRH Standards Program & IEC 60601

    Publisert: 7.11.2019
13. How to Embrace Risk for Safer Devices

    Publisert: 7.11.2019
14. Understanding The Differences Between Clearance vs Approval vs Granted

    Publisert: 7.11.2019
15. Streamlining The Device Marketing Authorization Process

    Publisert: 7.11.2019
16. How to Efficiently Raise Funds for Your Medical Device Company

    Publisert: 7.11.2019
17. The New Special 510(k)

    Publisert: 7.11.2019
18. What's New With PMAs

    Publisert: 7.11.2019
19. Career Tips for QA/RA Professionals in the Medical Device Industry

    Publisert: 7.11.2019
20. Why Design Verification Matters in Medical Device Design and Development

    Publisert: 7.11.2019