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现行 32017R1569
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Commission Delegated Regulation (EU) 2017/1569 of 23 May 2017 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections (Text with EEA relevance. ) 2017年5月23日的委员会授权法规(EU)2017/1569补充了欧洲议会和理事会第536/2014号法规(EU) 规定了供人类使用的试验药物良好生产规范的原则和指南以及检查安排(与EEA相关的文本)
发布日期: 2017-05-23
2017年5月23日的委员会授权法规(EU)2017/1569补充了欧洲议会和理事会第536/2014号法规(EU),规定了供人类使用的试验药物良好生产规范的原则和指南以及检查安排(与EEA相关的文本)
Commission Delegated Regulation (EU) 2017/1569 of 23 May 2017 supplementing Regulation (EU) No 536/2014 of the European Parliament and of the Council by specifying principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections (Text with EEA relevance. )
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