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Experts At US House Subcommittee Criticize FDA’s Initial Lack Of Serology Testing Oversight

The FDA’s initial lack of oversight of the tests shows why it is important for the agency to continue its public health responsibility in ensuring safe and effective products get to market, a panel of experts told lawmakers.

Coronavirus

A panel of experts brought together by a US House subcommittee criticized the US Food and Drug Administration’s decision to relax regulations early in the coronavirus pandemic – which the agency itself has admitted led to bad serology tests entering the market. In the past month, however, the FDA has tried to rectify the problem by issuing an updated guidance and pulling bad tests from shelves.

The Subcommittee on Economic and Consumer Policy under the House Committee on Oversight and Reform convened a 9 June panel...

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