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Emergency Use Authorization : ウィキペディア英語版 | Emergency Use Authorization An emergency use authorization (EUA), in the United States is a legal means for the Food and Drug Administration (FDA) to approve new drugs or new indications for previously approved drugs during a declared emergency.〔(U.S. Department of Health and Human Services, Food and Drug Administration, Office of the Commissioner, Office of Counterterrorism Policy and Planning ''Guidance: Emergency Use Authorization of Medical Products.'' July 2007. )〕 ==Response to swine influenza epidemic==
In response to requests from the U.S. Centers for Disease Control and Prevention, on April 27, 2009 the FDA issued Emergency Use Authorizations to make available diagnostic and therapeutic tools to identify and respond to the 2009 swine flu outbreak under certain circumstances. The agency issued these EUAs for the use of certain powerful antiviral drugs, and for the quantitative PCR Swine Flu test.〔(''FDA Authorizes Emergency Use of Influenza Medicines, Diagnostic Test in Response to Swine Flu Outbreak in Humans.'' FDA News, April 27, 2009. )〕
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「Emergency Use Authorization」の詳細全文を読む
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