Global Medical Device Podcast powered by Greenlight Guru

393 Jaksot

1. The Bleeding Edge: Lessons Learned for the Medical Device Industry

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

   Julkaistiin: 7.11.2019
3. 15 Habits of Highly Effective Regulatory Professionals

   Julkaistiin: 7.11.2019
4. What You Need to Know About The FDA CDRH Experiential Learning Program

   Julkaistiin: 7.11.2019
5. Latest Updates on CDRH Standards Program & IEC 60601

   Julkaistiin: 7.11.2019
6. Regulatory Tips & Observations from a Former FDA Reviewer

   Julkaistiin: 7.11.2019
7. How to Embrace Risk for Safer Devices

   Julkaistiin: 7.11.2019
8. Questions to Ask Before Hiring Your QA/RA Consultant

   Julkaistiin: 7.11.2019
9. What's New With PMAs

   Julkaistiin: 7.11.2019
10. Streamlining The Device Marketing Authorization Process

    Julkaistiin: 7.11.2019
11. How to Efficiently Raise Funds for Your Medical Device Company

    Julkaistiin: 7.11.2019
12. The New Special 510(k)

    Julkaistiin: 7.11.2019
13. Understanding The Differences Between Clearance vs Approval vs Granted

    Julkaistiin: 7.11.2019
14. Career Tips for QA/RA Professionals in the Medical Device Industry

    Julkaistiin: 7.11.2019
15. Implementing Changes to SaMD under New EU MDR

    Julkaistiin: 7.11.2019
16. Why Design Verification Matters in Medical Device Design and Development

    Julkaistiin: 7.11.2019
17. Leveraging Technology and Rapid Prototyping Methodologies during Product Development

    Julkaistiin: 7.11.2019
18. Understanding the Benefit-Risk Determinations of FDA's Latest Guidance Documents

    Julkaistiin: 7.11.2019
19. Is FDA's New 'Safer Technologies Program' Applicable To Your Medical Device?

    Julkaistiin: 7.11.2019
20. Addressing Top Questions of QA/RA Candidates on Salary, Skill Sets and Job Satisfaction

    Julkaistiin: 7.11.2019