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Marketing Authorization Application : ウィキペディア英語版 | Marketing Authorization Application Marketing Authorisation Application (MAA) is an application submitted by a drug manufacturer seeking permission to bring a newly developed medicinal product (for example, a new medicine) to the market. MAA is part of the official procedure before the Medicines and Healthcare products Regulatory Agency in the United Kingdom〔http://www.mhra.gov.uk/Howweregulate/Medicines/Licensingofmedicines/Marketingauthorisations/index.htm〕 and the Committee for Medicinal Products for Human Use of the European Commission. In the United States, the equivalent process is called New Drug Application. ==References==
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「Marketing Authorization Application」の詳細全文を読む
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