美国食品、药品和化妆品法案的历史以及医学的发展

Michael R. Hamrell
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引用次数: 2

摘要

未来药理学家在药物评估中的作用将随着科学知识和我们对药物和疾病过程的理解的增加而增加。此外,政治问题和公众的担忧将进一步要求科学界试图影响药物监管过程。FDA不断发布指令,指导药物开发的各个阶段,从确定一种化学物质作为治疗的潜在兴趣,到所有动物试验和临床阶段(4)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The history of the United States food, drug and cosmetic act and the development of medicine

The future role of pharmacologists in the evaluation of drugs will increase as scientific knowledge and our understanding of drugs and disease processes increase. In addition, political issues and public fears will place further demands on the scientific community to try to influence the drug regulatory process. The FDA continually issues directives which guide all phases of drug development, from the identification of a chemical as being of potential interest on therapy, through all animal tests and clinical phases (4).

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