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.
应对拟送进受核工厂的新组件、新物料、新化学品、新机器、新产品实施管制，以防对环境卫生安全有潜在损害的这些东西未经检验进入。
The controls should be in place to prevent new components, materials, chemicals, machinery, and products from entering the facility, which have not been reviewed for potential EHS hazards.
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