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Mutagenesis 17 , 471481 (2002)

If FDA follows the recommendation, it goes through formal rulemaking, which NPR reported could stretch into next year or 2028

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(Its worth noting that the committee was heavily made up of pro-peptide individuals, including doctors, and its also worth noting that the FDA itself advised against loosening restrictions, saying theres just not enough clinical evidence yet.) Approved peptides are thus eligible to be moved to the Section 503A Bulk List, which means compounding pharmacies could legally prepare said peptides for patientswith a valid prescription and specific quality and testing standards

10.1016/j.jbc.2021.100429 J