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The broader enforcement focus: Botox-type products, ophthalmics, clinical trials, recalls The RAPS article also highlights other key enforcement priorities for CDER in 2025: The agency issued 18 warning letters to firms marketing fraudulent or unapproved Botox-type products, warning that such products pose serious safety risks, including potential counterfeiting, incorrect/inactive ingredients, or falsification
Overcoming barriers and enabling artificial intelligence adoption in allied health clinical practice: a qualitative study
Disclosure: Compounded medications are not FDA-approved
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