European Medicines Agency (EMA) v MSD Animal Health Innovation GmbH and Intervet international BV.

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• European Medicines Agency (EMA) v MSD Animal Health Innovation GmbH and Intervet international BV.

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• Evonik Degussa GmbH v European Commission.
• European Commission v Federal Republic of Germany.
• European Medicines Agency (EMA) v AbbVie Inc. and AbbVie Ltd.
• European Commission v Republic of Malta.
• European Commission v Pilkington Group Ltd.



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• European Commission v Éditions Odile Jacob SAS.
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• AGC Glass Europe SA and Others v European Commission.
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• Regulation (EC) No 596/2009 of the European Parliament and of the Council of 18 June 2009 adapting a number of instruments subject to the procedure referred to in Article 251 of the Treaty to Council Decision 1999/468/EC with regard to the regulatory procedure with scrutiny — Adaptation to the regulatory procedure with scrutiny — Part Four
• 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 1049/2001 of the European Parliament and of the Council of 30 May 2001 regarding public access to European Parliament, Council and Commission documents
• Regulation (EU) No 1027/2012 of the European Parliament and of the Council of 25 October 2012 amending Regulation (EC) No 726/2004 as regards pharmacovigilance 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