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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)
发布日期: 2010-12-15
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,和第1394/2007号法规(EC)关于与欧洲经济区相关的先进治疗药物文本
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 EEA relevance
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