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At meetings scheduled for July 23 and 24 at the FDAs White Oak Campus in Silver Spring, Maryland, the FDAs Pharmacy Compounding Advisory Committee will consider whether to recommend adding seven peptide substances to the agencys 503A Bulks List, which would allow them to be used in certain compounded prescription drugs

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However, the effect of oral vitamin B 12 varies among patients (13), and the available randomized controlled trials comparing the two treatment regimens are considered to be of low quality (14)

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The FDA mandates that peptide manufacturers follow good manufacturing practices (GMPs) and conduct clinical trials to demonstrate the safety and efficacy of their products