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#323 The Combination Products Handbook

Global Medical Device Podcast powered by Greenlight Guru

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The Importance of Post-Market Safety Reporting in the FDA

The book goes through life cycle management of combination products from design transfer, all the way through what do you have to deal with post market. 21 CFR part four B is something that has challenged people in industry, although industries getting pretty good at it. There's also a challenge right now in that the US does do inspections on each constituent part for combination product when they do inspections. And then we're capped off by an appendix and glossary which is about 80 pages including links to all the different health authorities around the world.

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