Actavis Group PTC EHF (a company incorporated under the laws of Iceland) and Another v Boehringer Ingelheim Pharma Gmbh & Company, KG (a company incorporated under the laws of Germany)

Core Citations

CITES

• SmithKline Beecham Plc v Apotex Europe Ltd
• Actavis Group PTC EHF v Sanofi

CONSIDERS

• Patents Act 1977 - Articles : S-27

CITED in

• Warner-Lambert Company, LLC (Claimant) Actavis Group PTC EHF and Others (Defendants) National Health Service Commissioning Board (Respondent) Teva UK Ltd and Others (Interested Parties)

CONSIDERED in

• Bristol Myers Squibb Holdings Ireland Unlimited Company v Norton (Waterford) Ltd
• Bristol-Myers Squibb Holdings Ireland Unlimited Company v Patents Acts 1992 – 2019
• Merck Sharp & Dohme Ltd v Clonmel Healthcare Ltd

REFERRED in

• Bristol Myers Squibb Holdings Ireland Unlimited Company v Norton (Waterford) Ltd

This document cites

• SmithKline Beecham Plc v Apotex Europe Ltd
• Actavis Group PTC EHF v Sanofi
• Patents Act 1977
• Civil Procedure Rules 1998
• Medeva BV v Comptroller General of Patents, Designs and Trade Marks.



See all quotations

• 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)
• 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
• Commission Directive 1999/83/EC of 8 September 1999 amending the Annex to Council Directive 75/318/EEC on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of medicinal products (Text with EEA relevance)
• 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
• Commission Regulation (EC) No 469/2006 of 22 March 2006 establishing the standard import values for determining the entry price of certain fruit and vegetables