熱門推薦罰單破解實戰交通警察名師 25 年經驗,親授警察臨檢、檢舉魔人、科技執法、車禍糾紛的執法邏輯看課程介紹
購物車我的課程我的書籤免費註冊

Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use (Text with EEA relevance. ) ANNEX

ANNEX附則

ANNEX Correlation table Directive 2003/94/EC This Directive Commission Delegated Regulation (EU) 2017/1569 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections Article 1 Article 1 Article 1 Article 2 Article 2 Article 2 Article 3 Article 3 — Article 4 Article 4 Article 3 Article 5 Article 5 Article 4 Article 6 Article 6 Article 5(1) Article 7 Article 7 Article 6 Article 8 Article 8 Article 7 Article 9 Article 9 Article 8 Article 10 Article 10 Article 9 Article 11 Article 11 Article 10 Article 12 Article 12 Article 13 Article 13 Article 13 Article 14 Article 14 Article 14 Article 15 Article 15 — — Article 16 — — Article 17 — — Article 18 — — Article 19 — —

查看整部法規全文 →

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.