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.

Subject

Livestock

Keyword

Animal health Drugs Authorization/permit Internal trade

Geographical area

Eastern Europe, Europe, European Union Countries, Northern Europe

Abstract

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

Full text

English

Website

europa.eu

References - Legislation

Implemented by

Legislative Decree No. 119 implementing Directives Nos. 81/851/CEE, No. 81/852/CEE, No. 87/20/CEE and No. 90/676/CEE on veterinary drugs.

Legislation | Italy | 1992 (1997)

Keyword: Animal health, Drugs, Authorization/permit, International trade

Source: FAO, FAOLEX

Marketing Authorisations for Veterinary Medicinal Products Amendment Regulations 2000 (S.I. No. 776 of 2000).

Legislation | United Kingdom | 2000

Keyword: Non-edible products, Inspection, Quarantine, Pests/diseases, Transport/storage, Hygiene/sanitary procedures

Source: FAO, FAOLEX

Marketing Authorisations for Veterinary Medicinal Products Regulations 1994 (S.I. No. 3142 of 1994).

Legislation | United Kingdom | 1994

Keyword: Non-edible products, Inspection, Quarantine, Pests/diseases, Transport/storage, Hygiene/sanitary procedures

Source: FAO, FAOLEX

Animal Remedies Regulations, 1996.

Legislation | Ireland | 1996 | Repealed

Keyword: Animal health, Drugs, Authorization/permit, Internal trade, International trade, Inspection

Source: FAO, FAOLEX

Veterinary medicinal products (Presentation and content of license applications forms) Regulations 2002 (P.I. 200/2002).

Legislation | Cyprus | 2002

Keyword: Drugs, Authorization/permit, Registration, International trade

Source: FAO, FAOLEX

Amended by

Commission Directive 99/104/EC amending the Annex to Council Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products.

Legislation | European Union | 1999 | Repealed

Keyword: Animal health, Drugs

Source: FAO, FAOLEX

Council Directive 93/40/EEC amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products.

Legislation | European Union | 1993 | Repealed

Keyword: Drugs, Authorization/permit, Registration, Internal trade, International trade, Animal health

Source: FAO, FAOLEX

Repealed by

Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to veterinary medicinal products.

Legislation | European Union | 2001

Keyword: Basic legislation, Animal health, Drugs, Authorization/permit, Data collection/reporting, Access-to-information, Inspection, Institution, Internal trade, International trade, Offences/penalties

Source: FAO, FAOLEX