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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. )

C/2017/3368

Legal status of the documentIn force

CELEX number:
32017R1569
Form:
Delegated regulation
Responsible body:
SANTE
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
23/05/2017; Date of adoption
Number of pages:
10

Consolidated text: The consolidated text does not concern the English version.

CELEX number:
02017R1569-20170916
Form:
Consolidated text
Author:
Not available
Date of document:
16/09/2017
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Query: (PS_ID="reg_del:2017:1569:2017-09-16" OR (DTN_ELI=1569 AND DTA=2017 AND FM_CODED=REG_DEL AND DTC=false)) NOT ELI = NULL, Search language: German