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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 inspectionsText with EEA relevance.

32017R1569

Den Europæiske UnionForordning2017

European Union

Metadata

Type
Forordning
År
2017
Ikrafttrædelsesdato
1. januar 1970