EU GMP Annex 13/ Detailed Commission guidelines on good manufacturing practice for investigational medicinal products for human use, pursuant to the second subparagraph of Article 63(1) of Regulation (EU) No 536/2014

Title:
EU GMP Annex 13/ Detailed Commission guidelines on good manufacturing practice for investigational medicinal products for human use, pursuant to the second subparagraph of Article 63(1) of Regulation (EU) No 536/2014
Short Title:
GMP Guideliens for IMPs

https://www.gmp-compliance.org/files/guidemgr/guideline_adopted_1_en_act_part1_v3.pdf

Origin/Publisher:

EC Eudralex Volume 4

Document Type:
Guidelines
Content:
GMP Guideliens for IMPs

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