This database allows the user to access the public maximum residue limit assessment reports for active substances contained in veterinary medicines, which have been assessed by the European Medicines Agency's Committee for Medicinal Products for Veterinary Use (CVMP).
In the European Union, a maximum residue limit (MRL) is the maximum acceptable concentration of a substance that may be found in a food product obtained from an animal that has received a veterinary medicine.
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European Medicines Agency
European Medicines Agency 30 Churchill Place Canary Wharf London E14 5EU United Kingdom
Tel: +44 (0)20 3660 6000