Results (3620)
EMA has published an overview of its key recommendations of 2023 regarding the authorisation and safety monitoring of veterinary medicines.
The European Medicines Agency (EMA) has released a major revision of its user guide for micro, small, and medium-sized enterprises (SMEs) in the pharmaceutical sector.
In 2023, EMA recommended 77 medicines for marketing authorisation. Of these, 39 had a new active substance which had never been authorised in the European Union (EU) before.
Potential risk of neurodevelopmental disorders in children born to men treated with valproate medicines: PRAC recommends precautionary measures
EMA’s safety committee (PRAC) is recommending precautionary measures for the treatment of male patients with valproate medicines.
The midterm report of the European Medicines Agencies Network Strategy finds the pandemic strengthened the network and supported transformative change in the European system across key strategic areas.
The European Medicines Agency's (EMA) office is closed from Friday 22 December 2023 to Wednesday 3 January 2024. Outside of working hours and on public holidays, it is possible to call the product emergency hotline on +31(0)88 781 7600.
EMA's Executive Director, Emer Cooke, shares her end-of-year message and takes stock of EMA's work in 2023.
EMA and the Heads of Medicines Agencies (HMAs) have published an artificial intelligence (AI) workplan to 2028, setting out a collaborative and coordinated strategy to maximise the benefits of AI to stakeholders while managing the risks.