Global Medical Device Podcast powered by Greenlight Guru

416 Afleveringen

1. #334: MedTech Funding and Preparing for Due Diligence

   Gepubliceerd: 31-8-2023
2. #333: Exploring Breakthrough Device Designation

   Gepubliceerd: 25-8-2023
3. #332: Regulatory Strategy and the Advantage of Diversity in MedTech

   Gepubliceerd: 17-8-2023
4. #331: 28 Days To Save The World: Lessons Learned from a Pandemic Month of Supply Chain Issues

   Gepubliceerd: 10-8-2023
5. #330: 3P510k: What Is a 510k 3rd Party Review, and What are the Benefits?

   Gepubliceerd: 3-8-2023
6. #329 The Right Way to Start a QMS: When, How, & What

   Gepubliceerd: 27-7-2023
7. #328 FDA Guidance on Artificial Intelligence (AI) in Medical Devices

   Gepubliceerd: 20-7-2023
8. #327 Understanding the ROI of an eQMS

   Gepubliceerd: 11-7-2023
9. #326 CSA vs. CSV: Modern Validation for Modern MedTech

   Gepubliceerd: 7-7-2023
10. #325 The Role of dFMEAs in Risk Management for Medical Devices

    Gepubliceerd: 30-6-2023
11. #325 The Role of dFMEAs in Risk Management for Medical Devices

    Gepubliceerd: 29-6-2023
12. #324 Management Responsibility: The most important part of a QMS

    Gepubliceerd: 22-6-2023
13. #323 The Combination Products Handbook

    Gepubliceerd: 16-6-2023
14. Leaning into Lean Documentation

    Gepubliceerd: 7-6-2023
15. Cybersecurity and the Future of MedTech

    Gepubliceerd: 2-6-2023
16. How AI Can Help You Manage Risk

    Gepubliceerd: 26-5-2023
17. Ad Promo and The Difference in Regulatory & Legal

    Gepubliceerd: 24-5-2023
18. The Tools that Make Clinical Investigations

    Gepubliceerd: 13-5-2023
19. Complaint Handling with Medical Device Guru, Brittney McIver

    Gepubliceerd: 3-5-2023
20. Avoiding Potential Issues with your 510(k) Submission

    Gepubliceerd: 27-4-2023