The Queen, ex parte Rhône-Poulenc Rorer Ltd y May & Baker Ltd contra The Licensing Authority established by the Medicines Act 1968 (representada por The Medicines Control Agency).

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• The Queen, ex parte Rhône-Poulenc Rorer Ltd y May & Baker Ltd contra The Licensing Authority established by the Medicines Act 1968 (representada por The Medicines Control Agency).

This document cites

• Yearworth v Pierce
• Medicines Act 1968
• The Queen v The Licensing Authority established by the Medicines Act 1968 (acting by The Medicines Control Agency), ex parte Generics (UK) Ltd, The Wellcome Foundation Ltd and Glaxo Operations UK Ltd and Others.
• 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.
• The Queen contra Licensing Authority of the Department of Health y Norgine Ltd, ex parte Scotia Pharmaceuticals Ltd.



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• Comisión de las Comunidades Europeas contra República Federal de Alemania.
• Lucien Ortscheit GmbH contra Eurim-Pharm Arzneimittel GmbH.
• Comisión de las Comunidades Europeas contra República Federal de Alemania.
• Heinz Schumacher v Hauptzollamt Frankfurt am Main-Ost.
• Procedimento penal entablado contra Jean-Marie Delattre.
• Freistaat Bayern contra Eurim-Pharm GmbH.
• The Queen contra The Medicines Control Agency, ex parte Smith & Nephew Pharmaceuticals Ltd y Primecrown Ltd contra The Medicine Control Agency.
• Adriaan de Peijper, Managing Director of Centrafarm BV.
• United Kingdom of Great Britain and Northern Ireland v Commission of the European Communities.
• 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
• Council Directive 87/21/EEC of 22 December 1986 amending Directive 65/65/EEC on the approximation of provisions laid down by law, regulation or administrative action relating to proprietary medicinal products
• Treaty establishing the European Community