
PRAC carried out its responsibilities for managing risks associated with medicine use

Advice and guidance for manufacturers

Regulators, healthcare professionals and consumers working together

How the CVMP protects animal and public health

Health and environment agencies collaborate under One Health approach

Platform enables reporting on supply, demand and availability of medicines

Milestone highlights EMA's changing role in Europe
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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

Manufacturers can request advice on their medical device clinical development programme

Clinical Trials Information System now supports submission, assessment and oversight of all trials in the EU
EMA opinion for ivermectin and albendazole supports global efforts to eliminate widespread infections

Eight new medicines recommended for approval; one positive opinion for a medicine intended for use outside the EU
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This is a questions and answers (Q&A) session on the Product Management Service (PMS) Product User Interface (PUI) and Application Programming Interface (API).