Medtech Matters
A podcast by Medical Product Outsourcing
155 Episoade
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Should Wellness Products Come with a Warning?
Publicat: 11.09.2025 -
3 Most Common Premarket (Postmarket?) Review Issues FDA Sees
Publicat: 25.06.2025 -
Why Are One-Third of MAUDE Reports a Problem?
Publicat: 10.06.2025 -
FDA Guidance on Off-Label Communication, Part 1
Publicat: 30.05.2025 -
FDA Guidance on Off-Label Communication, Part 2
Publicat: 30.05.2025 -
Development Considerations for Over-the-Counter Medtech, Part 1
Publicat: 23.01.2025 -
Development Considerations for OTC Medtech, Part 2
Publicat: 23.01.2025 -
Device Descriptions in Regulatory Submissions
Publicat: 07.01.2025 -
Regulatory Ramifications Due to the Presidential Election
Publicat: 26.11.2024 -
Regulatory Considerations with an Assisted Suicide Machine
Publicat: 20.11.2024 -
Predetermined Change Control Plans, Part 2
Publicat: 24.09.2024 -
Predetermined Change Control Plans, Part 1
Publicat: 24.09.2024 -
What is a CAPA and How Do You Best Use It?
Publicat: 03.09.2024 -
You Got a 483 from the FDA. Now what?
Publicat: 22.08.2024 -
Revisiting Real-World Evidence
Publicat: 18.06.2024 -
The Most Dangerous Devices to Hit the Market
Publicat: 11.06.2024 -
Headline-Generating Medical Device Safety Concerns
Publicat: 02.05.2024 -
Analyzing ECRI’s 2024 Top 10 Health Technology Hazards
Publicat: 19.03.2024 -
Examining Institutional Review Boards
Publicat: 06.03.2024 -
Reimbursing Breakthrough Designation Products
Publicat: 02.01.2024
A podcast focused on the medical device technology industry, from design and development to outsourcing services and relationships to finished medtech products.
