AMENDMENTS 37 - 349 - Draft opinion Laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006
Committee on Industry, Research and Energy
Henna Virkkunen
Source : © European Union, 2023 - EP
Committee on Industry, Research and Energy
Henna Virkkunen
Source : © European Union, 2023 - EP