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In the United States, the traditional version of that practice is governed by section 503A of the Federal Food, Drug, and Cosmetic Act, which is why people call it "503A compounding." The defining features of 503A are that the work is patient-specific and prescription-driven

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doi:10.3945/jn.114.198010 Waegeneers N, Thiry C, De Temmerman L, Ruttens A