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

Date: 10.04.2024 · Reference: A9-0141/2024

pharmaceutical legislation security of supply approximation of laws investment promotion shortage European Medicines Agency medicinal product clinical trial antimicrobial resistance operation of the Institutions consumer information research and development market approval public health marketing standard
Overall Result: 459 Against
129 For
459 Against
1 Abstention
277 Did not vote
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