Medtech Matters

155 Episodes

1. Should Wellness Products Come with a Warning?

   Published: 11/09/2025
2. 3 Most Common Premarket (Postmarket?) Review Issues FDA Sees

   Published: 25/06/2025
3. Why Are One-Third of MAUDE Reports a Problem?

   Published: 10/06/2025
4. FDA Guidance on Off-Label Communication, Part 1

   Published: 30/05/2025
5. FDA Guidance on Off-Label Communication, Part 2

   Published: 30/05/2025
6. Development Considerations for Over-the-Counter Medtech, Part 1

   Published: 23/01/2025
7. Development Considerations for OTC Medtech, Part 2

   Published: 23/01/2025
8. Device Descriptions in Regulatory Submissions

   Published: 7/01/2025
9. Regulatory Ramifications Due to the Presidential Election

   Published: 26/11/2024
10. Regulatory Considerations with an Assisted Suicide Machine

    Published: 20/11/2024
11. Predetermined Change Control Plans, Part 2

    Published: 24/09/2024
12. Predetermined Change Control Plans, Part 1

    Published: 24/09/2024
13. What is a CAPA and How Do You Best Use It?

    Published: 3/09/2024
14. You Got a 483 from the FDA. Now what?

    Published: 22/08/2024
15. Revisiting Real-World Evidence

    Published: 18/06/2024
16. The Most Dangerous Devices to Hit the Market

    Published: 11/06/2024
17. Headline-Generating Medical Device Safety Concerns

    Published: 2/05/2024
18. Analyzing ECRI’s 2024 Top 10 Health Technology Hazards

    Published: 19/03/2024
19. Examining Institutional Review Boards

    Published: 6/03/2024
20. Reimbursing Breakthrough Designation Products

    Published: 2/01/2024