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GMP

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).

Organizations:
EC

Version Timeline

Chronological release history

2017-12-08

Version milestone

Publication Date

Dec 8, 2017

Effective Date

Not specified