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FDA's biosimilar drug approval push may delay due to USPTO patent dispute backlog.
The FDA’s initiative to accelerate the approval of biosimilar drugs, aimed at lowering costs and increasing access, may face delays due to challenges at the U.S. Patent and Trademark Office, which oversees patent disputes between generic and brand-name drug manufacturers.
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El impulso de la aprobación de medicamentos biosimilares de la FDA puede retrasarse debido a la acumulación de disputas de patentes de la USPTO.