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
| Amendments and corrections | |
|---|---|
| December 15, 2015 | Entry into force - Date pub. +20 See Art 19 |
| May 25, 2015 | Application - See Art 19 |
| Consolidated texts | ||
|---|---|---|
| November 25, 2014 | Date of publication | 32014R1252 |