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

    国会在1938年将顺势疗法药物确定管制产品这在联邦食品药品、化妆品法”明确规定。

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  • The hand sanitizing gel is an unapproved new drug under the Federal Food, Drug and Cosmetic Act and is therefore not permitted to be introduced into interstate commerce.

    手部消毒凝胶按《联邦食品药品化妆品法案》要求审批,因此允许进行际销售。

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  • The United States Congressional amendment to the Federal Food, Drug and Cosmetic Act - signed into law in May 2002 - eliminates any confusion regarding what is true ginseng.

    美国国会联邦食品药品化妆品修正案- 2002年5月签署成为法律-消除任何混乱关于什么真正人参

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  • 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.

    依据美国榀、榀、化让路法案501款以及美国药典国家处方的各中的含量测定和质量标准来构建法定标准。

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  • Importing and distributing unapproved drug products is a violation of the Federal Food, drug, and Cosmetic Act.

    任何司向美国进口销售这种未获得批准用于脂肪溶解术的药物行为都违反了美国食品药品化妆品法案。

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  • The seized products violate the Federal Food, Drug, and Cosmetic Act because they were held under insanitary conditions under which they may have become contaminated with filth.

    这些查封产品违反联邦食品药品化妆品法案,其贮藏条件不卫生,可能受到污染

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  • The current Good Manufacturing Practices (GMP) requirements set forth in the Quality System (QS) regulation are promulgated under section 520 of the Food, Drug and Cosmetic (FD&C) Act.

    质量体系法规所阐明的现行GMP要求食品药品化妆品法案第520节下所发布

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  • The current Good Manufacturing Practices (GMP) requirements set forth in the Quality System (QS) regulation are promulgated under section 520 of the Food, Drug and Cosmetic (FD&C) Act.

    质量体系法规所阐明的现行GMP要求食品药品化妆品法案第520节下所发布

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