EMA 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 Leave a Comment / By florent.maestracci / 31 January 2023 7 February 2023 https://health.ec.europa.eu/system/files/2017-12/guideline_adopted_1_en_act_part1_v3_0.pdf