Global Medical Device Podcast powered by Greenlight Guru

416 Episodo

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

   Publicado: 7/11/2019
2. How Human Factors Impact Your Medical Device

   Publicado: 7/11/2019
3. The Bleeding Edge: Lessons Learned for the Medical Device Industry

   Publicado: 7/11/2019
4. What you Need to Know about FDA's Progressive Programs

   Publicado: 7/11/2019
5. 15 Habits of Highly Effective Regulatory Professionals

   Publicado: 7/11/2019
6. How to Embrace Risk for Safer Devices

   Publicado: 7/11/2019
7. Latest Updates on CDRH Standards Program & IEC 60601

   Publicado: 7/11/2019
8. Questions to Ask Before Hiring Your QA/RA Consultant

   Publicado: 7/11/2019
9. What You Need to Know About The FDA CDRH Experiential Learning Program

   Publicado: 7/11/2019
10. Regulatory Tips & Observations from a Former FDA Reviewer

    Publicado: 7/11/2019
11. Understanding The Differences Between Clearance vs Approval vs Granted

    Publicado: 7/11/2019
12. What's New With PMAs

    Publicado: 7/11/2019
13. Streamlining The Device Marketing Authorization Process

    Publicado: 7/11/2019
14. How to Efficiently Raise Funds for Your Medical Device Company

    Publicado: 7/11/2019
15. The New Special 510(k)

    Publicado: 7/11/2019
16. Career Tips for QA/RA Professionals in the Medical Device Industry

    Publicado: 7/11/2019
17. Implementing Changes to SaMD under New EU MDR

    Publicado: 7/11/2019
18. Why Design Verification Matters in Medical Device Design and Development

    Publicado: 7/11/2019
19. Understanding the Benefit-Risk Determinations of FDA's Latest Guidance Documents

    Publicado: 7/11/2019
20. Leveraging Technology and Rapid Prototyping Methodologies during Product Development

    Publicado: 7/11/2019