要依据美国食榀、药榀、化让路法案501款以及美国药典和国家处方集的各论中的含量测定和质量标准来构建法定标准。
According to Section 501 of the Federal Food Drug and Cosmetic Act assays and specifications in monographs of the United States Pharmacopeia and the National Formulary constitute legal standards.
然而，这件事并没有发生，法案被修改延长最后限期，所以就减少了质量标准的“绝对性”。
This did not happen, however, and the Act has been amended to extend the deadlines, thereby reducing the "absolute" nature of the standards.
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