DRAFT REPORT
on the proposal for a regulation of the European Parliament and of the Council 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
(COM(2023)0193 - C9-0144/2023 - 2023/0131(COD))
Committee on the Environment, Public Health and Food Safety
Rapporteur: Tiemo Wölken

20.10.2023