
A new tool to respond rapidly to emerging animal and public health threats

PRAC carried out its broad range of responsibilities for managing the risks associated with medicine

Global regulators discuss how to support medicines development and approval

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How to improve quality of marketing authorisation application submissions
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Outcomes of the Committee for Veterinary Medicinal Products (CVMP) meeting.

Platform technologies enable rapid response to emerging infectious disease threats

PRAC carried out its broad range of responsibilities for managing the risks associated with medicine use
The European Medicines Agency's (EMA) office is closed on Friday 1 November 2024 for All Saints’ Day.

Global regulators discuss available knowledge supporting mpox medicine development and approval
Re-examination concludes effectiveness has not been confirmed
Events
The European Medicines Agency (EMA) is hosting a webinar on the next step in the resumption of the Clinical Data Publication (Policy 0070) activities.