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Two House Republicans on the China committee and an appropriations panel asked the FDA to bar Chinese trial data lacking a recent site audit, citing undisclosed deaths in Chinese gene-editing trials.
Why it’s here: A House Select Committee letter to FDA urging restrictions on China-generated clinical trial data in US drug applications is squarely a biotechnology policy item tied to China competition and FDA regulation.
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Aug 21CongressHouse Select Committee on the CCPTwo House Republicans on the China committee and an appropriations panel asked the FDA to bar Chinese trial data lacking a recent site audit, citing undisclosed deaths in Chinese gene-editing trials.BiotechDetails21 linked
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- China
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- Food and Drug Administration
- House Select Committee on the CCP