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FDA Issues Draft Guidance on 510(k)

Searcy Denney Scarola Barnhart & Shipley on 8/4/2014

The FDA issued a new draft guidance on July 15th which further explains how the FDA currently fails to protect consumers of medical devices and pharmaceutical drugs. It is important to remember that these sort of FDA-issued...more

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Risk Mitigation › Clinical Trials › Technology

FDA Issues Draft Guidance on 510(k)

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