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Medicines and Healthcare Products Regulatory Agency : ウィキペディア英語版 | Medicines and Healthcare Products Regulatory Agency
The Medicines and Healthcare Products Regulatory Agency (MHRA) is an executive agency of the Department of Health in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe. The Medicines and Healthcare Products Regulatory Agency was formed in 2003 with the merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA). In April 2013, it merged with the National Institute for Biological Standards and Control (NIBSC) and was rebranded, with the MHRA identity being used solely for the regulatory the centre within the group. The agency employs over 900 people.〔(【引用サイトリンク】 Working for us: MHRA )〕 ==Structure== The MHRA is divided into three main centres: * MHRA Regulatory (the regulator for the pharmaceutical and medical devices industries) * Clinical Practice Research Datalink * National Institute for Biological Standards and Control
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「Medicines and Healthcare Products Regulatory Agency」の詳細全文を読む
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