翻訳と辞書 Words near each other ・ Regulation of genetic engineering ・ Regulation of genetically modified organisms in Switzerland ・ Regulation of genetically modified organisms in the European Union ・ Regulation of greenhouse gases under the Clean Air Act ・ Regulation of hydraulic fracturing ・ Regulation of Interception of Communications and Provision of Communication-related Information Act, 2002 ・ Regulation of Investigatory Powers Act 2000 ・ Regulation of motorcycle access on freeways ・ Regulation of nanotechnology ・ Regulation of Railways Act 1868 ・ Regulation of Railways Act 1889 ・ Regulation of science ・ Regulation of ship pollution in the United States ・ Regulation of sport ・ Regulation of the release of genetically modified organisms ・ Regulation of therapeutic goods ・ Regulation of therapeutic goods in the United States ・ Regulation of tobacco by the U.S. Food and Drug Administration ・ Regulation of UAVs in the Republic of Ireland ・ Regulation of UAVs in the United States ・ Regulation of unmanned aerial vehicles ・ Regulation on Community designs ・ Regulation on Wholesale Energy Market Integrity and Transparency ・ Regulation Q ・ Regulation S-K ・ Regulation S-X ・ Regulation school ・ Regulation T ・ Regulation through litigation ・ Regulations for the Order and Discipline of the Troops of the United States Dictionary Lists mini英和辞書 mini和英辞書 Webster 1913 Latin-English FOLDOC Wikipedia English ウィキペディア

翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Regulation of therapeutic goods ： ウィキペディア英語版 Regulation of therapeutic goods The regulation of therapeutic goods, that is drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as is the case in Australia. The role of therapeutic goods regulation is designed mainly to protect the health and safety of the population. Regulation is aimed at ensuring the safety, quality, and efficacy of the therapeutic goods which are covered under the scope of the regulation. In most jurisdictions, therapeutic goods must be registered before they are allowed to be marketed. There is usually some degree of restriction of the availability of certain therapeutic goods depending on their risk to consumers. ==Regulation by country== 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「Regulation of therapeutic goods」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.