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MedicineVeterinaryAuthorised
Each month, the European Medicines Agency publishes an overview listing all safety signals discussed during the latest Pharmacovigilance Risk Assessment Committee (PRAC) meeting and the recommendations given for each of them. The overview includes PRAC recommendations for centrally and nationally authorised medicines.
HumanRegulatory and procedural guidancePharmacovigilance
PIPHuman
The European Medicines Agency (EMA) makes upgrades to this website from time to time, to improve user experience. During these upgrades, the website is unavailable for a short period of time, outside of EMA working hours. This page lists when we are planning the next outage and the main improvements made.
Corporate
PIPHuman
EventHumanData on medicines
PIPHuman
PIPHuman
OrphanHuman
OrphanHuman