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  Modernizing the FDA’s 510(k) Review Process: Pros, Cons and the Twilight Zone, Part 1

  December 12, 2018 By Alex Butler, Manager of Medical Device Solutions, MasterControl

  This blog post is the first of a series of three articles on the need to modernize the FDA’s 510(k) clearance process. Part 1 discusses key points of the ICIJ investigation on the medical device industry, the FDA’s response, and the implications of this hot-button public debate in the near future.

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