Santen SAS v Directeur général de l’Institut national de la propriété industrielle.

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• Santen SAS v Directeur général de l’Institut national de la propriété industrielle.

This document cites

• Andy Wightman and Others v Secretary of State for Exiting the European Union.
• Arne Forsgren v Österreichisches Patentamt.
• Pharmacia Italia SpA, formerly Pharmacia & Upjohn SpA.
• Neurim Pharmaceuticals (1991) Ltd v Comptroller-General of Patents.
• Relu Adrian Coman and Others v Inspectoratul General pentru Imigrări and Ministerul Afacerilor Interne.



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• Abraxis Bioscience LLC v Comptroller General of Patents.
• Synthon BV v Merz Pharma GmbH & Co. KGaA.
• Massachusetts Institute of Technology.
• Council Regulation (EEC) No 1768/92 of 18 June 1992 concerning the creation of a supplementary protection certificate for medicinal products
• 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 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (Codified version) (Text with EEA relevance)
• 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)
• Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use
• 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
• 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
• Consolidated version of the Treaty on the Functioning of the European Union 2016/C 202/01
• Directive 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to 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