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翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Drug Efficacy Study Implementation ： ウィキペディア英語版 Drug Efficacy Study Implementation Drug Efficacy Study Implementation (DESI) was a program begun by the Food and Drug Administration (FDA) in the 1960s after the requirement (in the Kefauver-Harris Drug Control Act) that all drugs be efficacious as well as safe, was made part of US law. The DESI program was intended to classify all pre-1962 drugs that were already on the market as either effective, ineffective, or needing further study.〔Pharmacy Today. August 2008. (FDA aims to remove unapproved drugs from market: Risk-based enforcement program focuses on removing potentially harmful products )〕 The Drug Efficacy Study Implementation (DESI) evaluated over 3000 separate products and over 16,000 therapeutic claims. By 1984, final action had been completed on 3,443 products; of these, 2,225 were found to be effective, 1,051 were found not effective, and 167 were pending. One of the early effects of the DESI study was the development of the Abbreviated New Drug Application (ANDA). == See also == * Estes Kefauver * Federal Food, Drug, and Cosmetic Act * Inverse benefit law * Regulation of therapeutic goods 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Drug Efficacy Study Implementation」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.