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FDA and CMS Make Case Before Congress for FDA Oversight of Laboratory Developed Tests

20 November 2015

Medical Device Alert

On November 17, 2015, leaders from both the Food and Drug Administration (FDA) and the Centers for Medicare & Medicaid Services (CMS) testified before the U.S. House of Representatives Committee on Energy and Commerce, Subcommittee on Health regarding regulation of Laboratory Developed Tests, or LDTs.

Read more: FDA and CMS Make Case Before Congress for FDA Oversight of Laboratory Developed Tests

The team

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