翻訳と辞書 Words near each other ・ Qualified Domestic Institutional Investor ・ Qualified domestic relations order ・ Qualified Flying Instructor ・ Qualified Foreign Institutional Investor ・ Qualified Health Benefit Plan ・ Qualified immunity ・ Qualified institutional buyer ・ Qualified institutional placement ・ Qualified intermediary ・ Qualified Lawyers Transfer Scheme ・ Qualified Lawyers Transfer Test ・ Qualified member of the engine department ・ Qualified New York political parties ・ Qualified Non-UK Pension Scheme ・ Qualified Performing Artist Deduction ・ Qualified person (European Union) ・ Qualified Person for Pharmacovigilance ・ Qualified Person Responsible For Pharmacovigilance ・ Qualified personal residence trust ・ Qualified privilege ・ Qualified Production Activities Income ・ Qualified prospect ・ Qualified residence interest ・ Qualified school construction bond ・ Qualified Security Assessor ・ Qualified specialist dyslexia teachers ・ Qualified Teacher Learning and Skills ・ Qualified Teacher Status ・ Qualified Through Verification ・ Qualified Weapons Instructor 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 Qualified person (European Union) ： ウィキペディア英語版 Qualified person (European Union) Qualified person (QP) is a technical term used in European Union pharmaceutical regulation (Directive 2001/83/EC for Medicinal products for human use). The regulations specify that no batch of medicinal product can be released for sale or supply prior to certification by a QP that the batch is in accordance with the relevant requirements.(EudraLex, Volume 4, Chapter 1) The QP is typically a licensed pharmacist, biologist or chemist (or a person with another permitted academic qualification) who has several years experience working in pharmaceutical manufacturing operations, and has passed examinations attesting to his or her knowledge. The requirement for QP oversight has been extended to material for use in clinical trials since the introduction of EU Directive 2001/20/EC. In countries that are part of the Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme (PIC/S), the same role may be termed responsible person (RP) or authorized person (AP). ==See also== * EudraLex * European Medicines Agency * EUDRANET * Ethics Committee * Clinical trial 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「Qualified person (European Union)」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.