This document is an excerpt from the EUR-Lex website
Document L:2017:238:TOC
Official Journal of the European Union, L 238, 16 September 2017
Official Journal of the European Union, L 238, 16 September 2017
Official Journal of the European Union, L 238, 16 September 2017
ISSN 1977-0677 |
||
Official Journal of the European Union |
L 238 |
|
![]() |
||
English edition |
Legislation |
Volume 60 |
Contents |
|
II Non-legislative acts |
page |
|
|
INTERNATIONAL AGREEMENTS |
|
|
* |
1 |
|
|
|
3 |
|
|
* |
8 |
|
|
* |
9 |
|
|
|
REGULATIONS |
|
|
* |
10 |
|
|
* |
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 ( 1 ) |
12 |
|
* |
22 |
|
|
* |
42 |
|
|
|
DIRECTIVES |
|
|
* |
Commission Directive (EU) 2017/1572 of 15 September 2017 supplementing Directive 2001/83/EC of the European Parliament and of the Council as regards the principles and guidelines of good manufacturing practice for medicinal products for human use ( 1 ) |
44 |
|
|
DECISIONS |
|
|
* |
51 |
|
|
|
ACTS ADOPTED BY BODIES CREATED BY INTERNATIONAL AGREEMENTS |
|
|
* |
53 |
|
|
Corrigenda |
|
|
* |
55 |
|
|
|
(1) Text with EEA relevance. |
EN |
Acts whose titles are printed in light type are those relating to day-to-day management of agricultural matters, and are generally valid for a limited period. The titles of all other Acts are printed in bold type and preceded by an asterisk. |