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

Changelog

0 versions

Article-level history is being prepared

The official source publishes these consolidated versions; article-by-article changes will appear here as soon as they are processed.

No consolidated versions are recorded for this law.