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UAE MOHAP has not listed peptide therapy as a drug, but neither has it prohibited it

It directly participates in methionine synthase reactions that convert homocysteine to methionine

These include congenital pernicious anaemia, Imerslund-Grsbeck Syndrome (caused by mutations in genes encoding cubulin and amnionless), inherited transcobalamin receptor (Haptocorrin) mutations, and intracellular cobalamin defects (CblA-CblG defects)

It sounds simple, almost trivial

This means BPC 157 peptide can enter the bloodstream within minutes, without first passing through the digestive system where stomach acid and enzymes might break it down

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