Eurlex法规编号: |
(EU) 2017/1569 |
OJ编号: |
OJ L 238, 16.9.2017, p. 12–21 |
中文标题: |
2017年5月3日委员会授权条例(EU) 2017/1569:补充欧洲议会和理事会条例(EU)No536/2014,制定人用试用药品的良好生产规范原则和准则及和安排安全检测 |
原文标题: |
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. ) |
发布日期 |
2017-09-16 |
原文链接 |
查看欧盟官网文件 |