The Medicines for Human Use (National Rules for Homoeopathic Products) Regulations 2006
2006年《人类用药（国家抗癌产品规则）》条例

The Medicines (Products for Human Use—Fees) Amendment Regulations 2000
2000年药物（人类使用费产品）修订规例

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