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

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