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On July 17, the Washington Post reported that FDA officials had raised concerns about appointing people who worked for peptide-related clinics and businesses

CowleySKoMPickNChowRDowningKJGordhanBGet al

Malmstrom K, Rodriguez-Gomez G, Guerra J, et al

The characteristics of all the original 320 patients will be recorded to provide insight into the type of patient left in the study after any withdrawals, as recommended by the CONSORT group [41, 42]