Reliable data on sales and use of antimicrobial medicinal products in animals help identify trends and possible risk factors for human and animal health.
EU / EEA Member States can use those insights to better design measures on the prudent use of antimicrobials, which can contribute to fight antimicrobial resistance. It can also help to evaluate the impact of those measures on public health.
EMA developed the platform under the Veterinary Medicinal Products Regulation (Article 57 of Regulation (EU) 2019/6).
EMA publishes the data that EU / EEA Member States report via this platform in annual reports. Reporting use data by animal species happens gradually, following an established reporting timeline.
For more information, including the annual reports and reporting timeline, see European Sales and Use of Antimicrobials for Veterinary Medicine (ESUAvet) annual surveillance reports.
From 2010 to 2023, Member States cooperated on a voluntary basis under the European Surveillance of Veterinary Antimicrobial Consumption (ESVAC) project.
All EU / EEA Member States must use the Antimicrobial Sales and Use Platform to report to EMA their data on the volume of sales and use of antimicrobial medicinal products in animals.
Use the link below to access the platform via the Union Product Database:
The platform only permits the upload of data in standardised formats.This enables data validation and automated calculation of antimicrobial amount.
All Member States must report their data in line with the relevant EU legislation:
EMA has made available five short video guides to help EU / EEA Member States access and use the platform.
Click on the titles below to access the videos.
Guidance is available to help national competent authorities implement the legislative requirements for reporting sales and use of antimicrobial medicinal products in animals.
These documents, developed by EMA with experts from the EU / EEA network, contain the technical specifications that Member States need to on the sales and use of antimicrobial medicinal products in animals. The specifications are in line with the legislation.
EMA will make updated versions of these documents available in a timely manner.
EMA makes available the necessary protocols and templates for EU / EEA national competent authorities to report data on antimicrobials sales, use and animal populations:
Other supporting materials for national competent authorities are available in the EU Network Training Centre (EU NTC), including webinar recordings.