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Where drugmakers have to identify the manufacturer thatll supply their materials in their FDA drug application and have them inspected (and will also typically do their own regular testing to verify what they receive), compounders just need to get ingredients from an FDA-registered facility, a.k.a
Retatrutide is still investigational and hasnt been submitted to the MHRA, the FDA, or any other regulator for approval
In September 2023, the FDA moved more than a dozen commonly compounded peptides into Category 2 of the 503A bulks list a designation for substances with significant safety concerns, which effectively stopped licensed pharmacies from compounding them
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