Commission of the European Communities v Artegodan GmbH.

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• Commission of the European Communities v Artegodan GmbH.

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• Emesa Sugar (Free Zone) NV v Commission of the European Communities.
• Upjohn Ltd v The Licensing Authority established by the Medicines Act 1968 and Others.
• Comisión de las Comunidades Europeas contra Atlantic Container Line AB y otros.
• Commission of the European Communities v Gerot Pharmazeutika GmbH.
• Commission of the European Communities v Schuck GmbH.



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• Commission of the European Communities v Laboratórios Roussel Ldª and Laboratoires Roussel Diamant SARL.
• TWD Textilwerke Deggendorf GmbH contra Bundesrepublik Deutschland.
• Commission of the European Communities v Laboratórios Roussel Ldª and Roussel Iberica SA.
• Commission of the European Communities v Bruno Farmaceuitici SpA and Others.
• Procedimento penal entablado contra Johannes Stephanus Wilhelmus Ter Voort.
• Comisión de las Comunidades Europeas contra AssiDomän Kraft Products AB, Iggesunds Bruk AB, Korsnäs AB, MoDo Paper AB, Södra Cell AB, Stora Kopparbergs Bergslags AB y Svenska Cellulosa AB.
• Commission of the European Communities v Cambridge Healthcare Supplies Ltd.
• Reino de los Países Bajos contra Consejo de la Unión Europea.
• Commission of the European Communities v Hänseler GmbH.
• Commission of the European Communities v Laboratoires pharmaceutiques Trenker SA.
• 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 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products
• Council Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products
• 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
• Council Directive 89/341/EEC of 3 May 1989 amending Directives 65/65/EEC, 75/318/EEC and 75/319/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products
• Commission Directive 91/507/EEC of 19 July 1991 modifying the Annex to Council Directive 75/318/EEC on the approximation of the laws of Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of medicinal products
• Treaty establishing the European Community