Medtech Matters

Medtech Matters

Por: Medical Product Outsourcing
A podcast focused on the medical device technology industry, from design and development to outsourcing services and relationships to finished medtech products.
154 episodios disponibles

Latest episodes of the podcast Medtech Matters

Should Wellness Products Come with a Warning? 11/09/2025
3 Most Common Premarket (Postmarket?) Review Issues FDA Sees 25/06/2025
Why Are One-Third of MAUDE Reports a Problem? 10/06/2025
FDA Guidance on Off-Label Communication, Part 2 30/05/2025
FDA Guidance on Off-Label Communication, Part 1 30/05/2025
Development Considerations for OTC Medtech, Part 2 23/01/2025
Development Considerations for Over-the-Counter Medtech, Part 1 23/01/2025
Device Descriptions in Regulatory Submissions 07/01/2025
Regulatory Ramifications Due to the Presidential Election 26/11/2024
Regulatory Considerations with an Assisted Suicide Machine 20/11/2024
Predetermined Change Control Plans, Part 2 24/09/2024
Predetermined Change Control Plans, Part 1 24/09/2024
What is a CAPA and How Do You Best Use It? 03/09/2024
You Got a 483 from the FDA. Now what? 22/08/2024
Revisiting Real-World Evidence 18/06/2024
The Most Dangerous Devices to Hit the Market 11/06/2024
Headline-Generating Medical Device Safety Concerns 02/05/2024
Analyzing ECRI’s 2024 Top 10 Health Technology Hazards 19/03/2024
Examining Institutional Review Boards 06/03/2024
Reimbursing Breakthrough Designation Products 02/01/2024
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