Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance)
2004年3月31日欧洲议会和理事会第2004/27/EC号指令 修订了关于人类使用医药产品的共同体规范的第2001/83/EC号指令（与欧洲经济区相关的文本）

2004-03-31

Directive 2008/29/EC of the European Parliament and of the Council of 11 March 2008 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the implementing powers conferred on the Commission
欧洲议会和理事会2008年3月11日第2008/29/EC号指令 修订了关于人类用医药产品共同体规范的第2001/83/EC号指令

2008-03-11

Directive 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products Text with EEA relevance
欧洲议会和理事会2011年6月8日第2011/62/EU号指令修订了关于人类使用的医药产品的共同体代码的第2001/83/EC号指令 该指令涉及防止与欧洲经济区相关的伪造医药产品文本进入合法供应链

2011-06-08

Regulation (EU) 2019/5 of the European Parliament and of the Council of 11 December 2018 amending Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, Regulation (EC) No 1901/2006 on medicinal products for paediatric use and Directive 2001/83/EC on the Community code relating to medicinal products for huma
2018年12月11日欧洲议会和理事会第2019/5号法规（EU）修订了第726/2004号法规（EC） 规定了共同体对人用和兽医用药品的授权和监督程序 并成立了欧洲药品管理局 关于儿科用药的第1901/2006号法规（EC）和关于人体用药的共同体规范的第2001/83/EC号指令

2018-12-11