The Medicines for Human Use (Marketing Authorisations Etc.) Amendment Regulations 2005
2005年人类用药（销售许可等）修订条例

The Medicines for Human Use (Marketing Authorisations Etc.) Amendment Regulations 2000
2000年人类用药（销售许可等）修订规例

The Medicines for Human Use (Marketing Authorisations Etc.) Amendment Regulations 2003
2003年人类用药（上市许可等）修订规例

The Medicines for Human Use (Marketing Authorisations Etc.) Amendment Regulations 2009
2009年人类用药（销售许可等）修订条例

The Medicines (Marketing Authorisations Etc.) Amendment Regulations 2005
2005年药品（销售许可等）修订条例

Regulation (EU) No 1235/2010 of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance of medicinal products for human use, 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, and Regulation (EC) No 1394/2007 on advanced therapy medicinal products Text with
2010年12月15日 欧洲议会和理事会第1235/2010号法规（EU）修订了关于人用药品的药物警戒的第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 和（EC）第1394/2007号法规（关于高级治疗药物产品的文本 带E）

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