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The US Food and Drug Administration (FDA) has issued 30 warning letters to telehealth companies for false or misleading marketing claims about 1 Regulators allege that the telehealth firms made unsubstantiated assertions about compounded GLP-1 RA products, including claims implying comparability to approved therapies, such as semaglutide- or tirzepatide-based medications, and about their safety or effectiveness

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