Maximum residue limit assessment reports

The European Medicines Agency (EMA) publishes assessment reports on maximum residue limits for active substances contained in veterinary medicines, which have been assessed by the EMA's Committee for Medicinal Products for Veterinary Use (CVMP) and are currently pending the adoption of a legally binding Regulation by the European Commission.

Last updated:
VeterinaryRegulatory and procedural guidanceMaximum residue limitMedicinesResearch and development