Linda Svitak

Linda Svitak

Faegre Drinker Biddle & Reath LLP

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Latest Posts › Food and Drug Administration (FDA)

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FDA House Legislation Would Relax Reporting of Medical Device Malfunctions

On July 12, 2017, the U.S. House of Representatives passed a bill to reauthorize four of the U.S. Food and Drug Administration’s user fees and to change various drug and device testing rules. H.R. 2430 – the FDA...more

7/18/2017  /  FDA Reauthorization Act , Food and Drug Administration (FDA) , Medical Devices , User Fees
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