国会在1938年将顺势疗法药物确定为受管制产品。 这在“联邦食品、药品、化妆品法”中有明确规定。

Congress recognized Homeopathic Drugs as a class of regulated products 1938, with the passage of the Federal Food, Drug and Cosmetic Act.

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FDA建议彻底修正已过时的1906年《食品和药品法》。从第一项议案提交给参议院开始，开始了一场为期五年的立法之战。

FDA recommends a complete revision of the obsolete 1906 Food and Drugs Act. The first bill is introduced into the Senate, launching a five-year legislative battle.

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建立了罗红霉素新的TLC法，并与《日本抗生物质医药品基准解说》1993年版收载的方法进行了比较。

A novel TLC method of roxithromycin was compared with the TLC method which was described in "the Japanese Standards of Antibiotics (1993)".

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