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#USA #safety #health To view or add a comment, sign in "According to the regulator, applicants who conduct any required bioequivalence testing in the US, and whose products are made there using exclusively domestic sources for active pharmaceutical ingredients (APIs), will be eligible for priority review." "In a statement announcing the scheme, the FDA said that more than half of the pharmaceuticals distributed in the US are manufactured overseas, while only 9% of APIs are produced domestically
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