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The Therapeutic Goods Administration has issued a safety warning, saying it's "concerned" about an increase in the importation and supply of unapproved peptides. Since January 2026, there have been six cases of acute liver toxicity associated with unapproved peptide products labelled Retatrutide in Australia. These toxic effects may be linked to a contaminant in the Classifying active medical devices in Australia (including software based medical devices) Therapeutic Goods Administration (TGA) Peptides Are Now on the TGA's Radar. Is Your Clinic Ready?

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