French Republic v Monsanto Company and Commission of the European Communities.

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• French Republic v Monsanto Company and Commission of the European Communities.

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• The Queen contra Ministry of Agriculture, Fisheries and Food, Commissioners of Customs & Excise, ex parte National Farmers' Union, David Burnett and Sons Ltd, R. S. and E. Wright Ltd, Anglo Beef Processors Ltd, United Kingdom Genetics, Wyjac Calves Ltd, International Traders Ferry Ltd, MFP International Ltd, Interstate Truck Rental Ltd y Vian Exports Ltd.
• Heinz-Jörg Moritz contra Comisión de las Comunidades Europeas.
• Reino Unido de Gran Bretaña y de Irlanda del Norte contra Comisión de las Comunidades Europeas.
• Antillean Rice Mills NV, European Rice Brokers AVV y Guyana Investments AVV contra Comisión de las Comunidades Europeas.
• Reino de los Países Bajos contra Consejo de la Unión Europea.



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• República Italiana contra Comisión de las Comunidades Europeas.
• Pedro Bocos Viciano v Commission of the European Communities.
• Dutch Antillian Dairy Industry Inc. y Verenigde Douane-Agenten BV contra Rijksdienst voor de keuring van Vee en Vlees.
• Jan Robert de Rijk contra Comisión de las Comunidades Europeas.
• 91/664/EEC: Council Decision of 11 December 1991 designating the Community reference laboratories for testing certain substances for residues
• Council Directive 93/39/EEC of 14 June 1993 amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC in respect of medicinal products
• Council Directive 86/469/EEC of 16 September 1986 concerning the examination of animals and fresh meat for the presence of residues
• Council Regulation (EC) No 1308/1999 pf 15 June 1999 amending Regulation (EC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin
• 90/218/EEC: Council Decision of 25 April 1990 concerning the administration of Bovine Somatotrophin (BST)
• Council Regulation (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products
• 94/936/EC: Council Decision of 20 December 1994 amending Decision 90/218/EEC concerning the placing on the market and administration of bovine somatotrophin (BST)
• Council Directive 96/23/EC of 29 April 1996 on measures to monitor certain substances and residues thereof in live animals and animal products and repealing Directives 85/358/EEC and 86/469/EEC and Decisions 89/187/EEC and 91/664/EEC
• 1999/879/EC: Council Decision of 17 December 1999 concerning the placing on the market and administration of bovine somatotrophin (BST) and repealing Decision 90/218/EEC
• Council Directive 85/358/EEC of 16 July 1985 supplementing Directive 81/602/EEC concerning the prohibition of certain substances having a hormonal action and of any substances having a thyrostatic action
• 89/187/EEC: Council Decision of 6 March 1989 determining the powers and conditions of operation of the Community reference laboratories provided for by Directive 86/469/EEC concerning the examination of animals and fresh meat for the presence of residues
• Council Directive 93/40/EEC of 14 June 1993 amending Directives 81/851/EEC and 81/852/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products
• Council Directive 87/22/EEC of 22 December 1986 on the approximation of national measures relating to the placing on the market of high-technology medicinal products, particularly those derived from biotechnology
• 92/88/EEC: Commission Decision of 9 January 1992 approving the plan concerning infectious haemopoietic necrosis and viral haemorrhagic septicaemia presented by Greece (Only the Greek text is authentic)
• Council Directive 92/46/EEC of 16 June 1992 laying down the health rules for the production and placing on the market of raw milk, heat-treated milk and milk-based products
• Council Directive 81/852/EEC of 28 September 1981 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 81/851/EEC of 28 September 1981 on the approximation of the laws of the Member States relating to veterinary medicinal products
• Treaty establishing the European Community