Modified standards and protocols for testing veterinary medicinal products
Commission Directive 92/18/EEC of 20.3.1992 modifies the Annex to Council Directive 81/852/EEC of 28.9.1981 on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of veterinary medicinal products. Its aim is firstly to amend the Annex to include special requirements for the testing of immunological veterinary medicinal products (encompassing analytical testing, safety testing, and efficacy trials), and secondly to adapt to technical progress the existing requirements laid down in the Annex.