Global Medical Device Podcast powered by Greenlight Guru

416 Episodes

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

   Published: 8/31/2023
2. #333: Exploring Breakthrough Device Designation

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

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

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

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

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

   Published: 7/20/2023
8. #327 Understanding the ROI of an eQMS

   Published: 7/11/2023
9. #326 CSA vs. CSV: Modern Validation for Modern MedTech

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

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

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

    Published: 6/22/2023
13. #323 The Combination Products Handbook

    Published: 6/16/2023
14. Leaning into Lean Documentation

    Published: 6/7/2023
15. Cybersecurity and the Future of MedTech

    Published: 6/2/2023
16. How AI Can Help You Manage Risk

    Published: 5/26/2023
17. Ad Promo and The Difference in Regulatory & Legal

    Published: 5/24/2023
18. The Tools that Make Clinical Investigations

    Published: 5/13/2023
19. Complaint Handling with Medical Device Guru, Brittney McIver

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

    Published: 4/27/2023