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EMA and HMA encourage strengthening Europe’s production capacity
Outcomes of the Committee for Veterinary Medicinal Products (CVMP) meeting
PRAC carried out its broad range of responsibilities for managing the risks associated with medicine use
Yearly updates to virus strains ensure vaccine effectiveness
Designation facilitates data sharing, promotes transparency and trust in clinical research
Proposal aims to encourage development and improve patient access
Data comes from EU27 plus Iceland and Norway
Benefits continue to outweigh risks, with new risk minimisation measures and more information to be provided about long-term effect on the heart
Five new medicines recommended for approval; another seven medicines recommended for extension of their therapeutic indications
Manufacturers can request advice on their medical device clinical development programme