Neurim Pharmaceuticals (1991) Ltd v The Comptroller-General of Patents

Core Citations

CONSIDERS

RESUELVE RECURSO

• Neurim Pharmaceuticals (1991) Ltd v The Comptroller-General of Patents

CONSIDERS

• Yissum Research and Development Company of the Hebrew University of Jerusalem v Comptroller-General of Patents

CITED in

• Merck Serono S.A. v The Comptroller-General of Patents, Designs and Trade Marks

REFERRED in

• Newron Pharmaceuticals S.P.A. v The Comptroller General of Patents, Trademarks and Designs

REPORTED OPINION OF in

• 2011 RPC 19

CONSIDERED in

• Abraxis Bioscience LLC v The Comptroller-General of Patents
• Glaxosmithkline Biologicals Sa v Comptroller-general of Patents, Designs and Trade Marks

This document cites

• Yissum Research and Development Company of the Hebrew University of Jerusalem v Comptroller-General of Patents
• Neurim Pharmaceuticals (1991) Ltd v Comptroller-General of Patents
• AHP Manufacturing BV v Bureau voor de Industriële Eigendom.
• Hogan Lovells International LLP v Bayer CropScience AG.
• Council Regulation (EEC) No 1768/92 of 18 June 1992 concerning the creation of a supplementary protection certificate for medicinal products



See all quotations

• 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
• 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
• Regulation (EC) No 1610/96 of the European Parliament and of the Council of 23 July 1996 concerning the creation of a supplementary protection certificate for plant protection 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