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Marty Makary posted on X that the FDA will take swift action against companies mass-marketing illegal copycat drugs, claiming they are similar to FDA-approved products. He emphasized that the FDA cannot verify the quality, safety, or effectiveness of non-approved drugs. The agency also issued a news release indicating that Hims would be among the companies subject to scrutiny

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That means planning for flexibility and designing facilities that will support next-generation manufacturing innovations, including aqueous-based synthesis and a shift from injectables to oral tablets

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