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 2004/24/EC of the European Parliament and of the Council of 31 March 2004 amending, as regards traditional herbal medicinal products, Directive 2001/83/EC on the Community code relating to medicinal products for human use
欧洲议会和理事会2004年3月31日第2004/24/EC号指令 就传统草药产品修订了关于人类用医药产品的共同体规范的第2001/83/EC号指令

2004-03-31

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 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

Commission Directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use (Text with EEA relevance)
2003年6月25日的委员会指令2003/63/EC 修订了欧洲议会和理事会关于人类使用医药产品的共同体规范的指令2001/83/EC（与欧洲经济区相关的文本）

2003-06-25

Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use Text with EEA relevance
2010年12月15日欧洲议会和理事会第2010/84/EU号指令修订了关于药物警戒的第2001/83/EC号指令 该指令涉及与欧洲经济区相关的人类使用药品文本的共同体代码

2010-12-15

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

Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (Text with EEA
2009年5月6日欧洲议会和理事会第470/2009号法规（EC）规定了制定动物源性食品中药理活性物质残留限量的共同体程序 废除第2377/90号理事会条例（EEC）并修订欧洲议会和理事会第2001/82/EC号指令以及欧洲议会和理事会第726/2004号条例（EC）（与EEA的文本）

2009-05-06

Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use Text with EEA relevance
2014年5月28日第1252/2014号委员会授权法规（EU）补充了欧洲议会和理事会指令2001/83/EC 涉及与EEA相关的人用医药产品活性物质良好生产规范的原则和指南

2014-05-28

Commission Regulation (EC) No 1950/2006 of 13 December 2006 establishing, in accordance with Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products, a list of substances essential for the treatment of equidae (Text with EEA relevance)
2006年12月13日第1950/2006号委员会条例（EC） 根据欧洲议会和理事会关于兽药产品的共同体规范的指令2001/82/EC 制定了治疗马科动物所必需的物质清单（与欧洲经济区相关的文本）

2006-12-13