[2019] PTSR 1642

Core Citations

REPORTS OPINION

• Orion Corporation v The Secretary of State for Health and Social Care Acting as the Licensing Authority

This document cites

• The Queen (on the application of Napp Pharmaceuticals Ltd) v Secretary of State for Health acting as the Licensing Authority Sandoz Ltd (Interested Party)
• Trinity Mirror Plc (formerly Mirror Group Newspapers Ltd) v Commissioners of Customs and Excise
• Capernwray Missionary Fellowship of Torchbearers v Revenue and Customs Commissioners
• Coal Staff Superannuation Scheme Trustees Ltd v Revenue and Customs Commissioners
• The Queen contra Licensing Authority of the Department of Health y Norgine Ltd, ex parte Scotia Pharmaceuticals Ltd.



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• Malika Tennah-Durez v Conseil national de l'ordre des médecins.
• Novartis Europharm Ltd v European Commission.
• Arthur Wiedemann v Land Baden-Württemberg (C-329/06) and Peter Funk v Stadt Chemnitz (C-343/06).
• H. Lundbeck A/S and Lundbeck Ltd v European Commission.
• Olainfarm AS v Latvijas Republikas Veselības ministrija and Zāļu valsts aģentūra.
• The Queen v Ministry of Agriculture, Fisheries and Food, ex parte: Hedley Lomas (Ireland) Ltd.
• Proceedings brought by Astellas Pharma GmbH.
• Wiener S.I. GmbH contra Hauptzollamt Emmerich.
• Comisión de las Comunidades Europeas contra República Italiana.
• Ditta Angelo Celestini contra Saar-Sektkellerei Faber GmbH & Co. KG.
• The Queen, on the application of Generics (UK) Ltd v Licensing Authority.
• European Commission v Republic of Lithuania.
• Criminal proceedings against Karl Schwarz.
• Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
• Regulation (EC) No 1901/2006 of the European Parliament and of the Council of 12 December 2006 on medicinal products for paediatric use and amending Regulation (EEC) No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation (EC) No 726/2004 (Text with EEA relevance)
• 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
• Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)Text with EEA relevance
• Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004 (Text with EEA relevance)
• Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance)