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Learn more about EMA's Committee for Veterinary Medicinal Products (CVMP) and its role in veterinary medicine regulation in Europe.

Featured information for animal health professionals

EMA joins EU Partnership on Animal Health and Welfare

EMA has become an associate of the EU Partnership on Animal Health and Welfare, established to help control infectious diseases of both terrestrial and aquatic animals. This partnership also aims to support the global One Health initiative. In this capacity, EMA will strengthen links between research and EU medicines regulation through communication and engagement with researchers and other stakeholders.

Promoting a One Health approach in Europe

EMA and other scientific EU agencies responsible for human, animal health and environmental protection have issued a joint statement on promoting a joined-up One Health agenda in Europe. They identify four priority areas for action.

EMA recommendations to reduce risks to humans and animals from exposure to N-methyl pyrrolidone in veterinary medicines

EMA’s Committee for Veterinary Medicinal Products (CVMP) recommended measures addressing the inconsistencies in the product information of medicines containing the excipient N-methyl pyrrolidone (NMP), which are marketed in the European Union (EU). NMP can cause birth defects in children of women who handle NMP-containing medicines during pregnancy, and in the offspring of animals given these medicines

Stay safe when buying veterinary medicines online

From 28 January 2022, you can check if an online retailer is authorised to sell veterinary medicines in the EU / EEA by looking for the official logo on the retailer's website. Clicking on the logo should open the national register where the retailer is established and registered. Do not continue with your purchase if the retailer is not on the national register.

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Upcoming events

Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - July 2024

The Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) was established under Regulation 2022/123 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices.

Online
European Medicines Agency, Amsterdam, the Netherlands
Start date: 1 July 2024, 09:30 (CEST)
End date: 1 July 2024, 11:45 (CEST)
EventHumanVeterinaryMedicine shortagesMedicines
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Publications of interest

EMA's 2023 annual report

Navigate through the digital report to view interviews, short videos and an interactive timeline of the Agency’s main activities in 2023. Read the traditional PDF version to see additional figures and statistics on EMA's regulatory procedures and activities.

10-year report on EMA's MUMS / veterinary limited market scheme

Read about the main achievements of EMA's MUMS / veterinary limited market scheme during its period of application. The scheme has since been replaced by specific legal provisions for veterinary limited markets in the Veterinary Medicines Regulation, which came into effect in January 2022.

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