Detailed Commission guideline of 8 December 2017 on the good manufacturing practice for investigational medicinal products pursuant to the second paragraph of the Article 63(1) of Regulation (EU) No 536/2014

Imported from European Commission — EudraLex (https://health.ec.europa.eu/medicinal-products/eudralex/eudralex-volume-4_en).

Organisaties:

EC