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. )
Amendments and corrections
October 6, 2017 Entry into force - Date pub. +20 See Art 27
January 1, 1001 Application - See Art 27
Consolidated texts
September 16, 2017 Date of publication 32017R1569