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Home»Law and Cases»Legislation»Council Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products.
Council Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products.
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Member States shall take all appropriate measures to ensure that the particulars and documents which shall accompany applications for authorization to place a veterinary medicinal product on the market, pursuant article 5 of Directive 81/851/EC, are submitted by the persons concerned in accordance with the Annex to this Directive. The Annex is divided in 3 parts: analytical (physico-chemical, biological or microbiological) tests of veterinary medicinal products (I), toxicological and pharmacolog
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Council Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products.
