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Listen to the full episode → Regulatory pressure: FDA’s 2026 crackdown As GLP-1 demand outpaced approved supply between 2022 and 2025, compounded and counterfeit versions proliferated and FDA enforcement has intensified sharply in response: FDA’s Center for Drug Evaluation and Research issued 303 warning letters to drug and biologics manufacturers in fiscal year 2025, a 59% increase from 190 in FY2024, according to an analysis of inspection and enforcement trends
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