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If the peptide restrictions are reversed through formal FDA rulemaking, compounding pharmacies would be legally allowed to prepare those peptides, but only as traditional, patient-specific compounded drugs, not as mass-market or FDA-approved therapies. If the peptides are formally added to the 503A bulk list, he says, pharmacies would have to follow the traditional 503A compounding rules

The appearance of different forms of GGT in clinical chemistry testing appears to be attributed to variation in the N-terminal structure, which is due to non-specific limited proteolysis as well as to an association with exosomes [80] and/or simply to the structures of glycans [82]

You can see my testimony at the PCAC if you watch the live stream or the pre-recorded version on youtube at: Also our 5 risks of peptides, like bpc-157, is a useful resource in this area: I really think the FDA will ultimately ignore the opinion of the largely financially conflicted PCAC

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