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The European Medicines Agency's scientific guidelines on the availability of immunologicals help medicine developers prepare marketing authorisation applications for veterinary medicines.
The European Medicines Agency (EMA) publishes summaries of opinion 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.
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.