In September 2006 an Institute of Medicine (IOM) ad hoc committee on the Assessment of the US Drug Safety System released its report entitled "The Future of Drug Safety: Promoting and Protecting the Health of the Public". The committee's report includes 25 recommendations that "will bring the strengths of the preapproval process (data, regulatory authority, organizational function and capabilities, and resources) to the postapproval phase in order to fulfill a lifecycle approach to the study, regulation, and communication about the risks and benefits of drugs." Copies of the report are available from the National Academies Press (800-624-6242), and the full text is available at http://www.nap.edu.

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2006年9月,美国医学研究所 (IOM) 评估美国药物安全体系特设委员会发布了题为 “药物安全的未来: 促进和保护公众健康” 的报告。该委员会的报告包括25项建议,“将把预批准过程的优势 (数据、监管机构、组织职能和能力以及资源) 带到后批准阶段,以实现研究、监管和药物风险和益处沟通的生命周期方法。”该报告的副本可从国家科学院出版社 (800-624-6242) 获得,全文可在http://www.nap.edu获得。

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