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Bill would cut regulatory red tape in U.S. for medical devices (access required)

Legislation that would streamline the regulatory process for some medical devices has been filed in the Senate. The Medical Device Regulatory Improvement Act, S. 1700, introduced by Sens. Amy Klobuchar, D-Minn., Richard Burr, R-N.C., and Michael Bennet, D-Colo., would streamline the Food and Drug Administration’s regulation process for certain medical devices by clarifying some of ...

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