Pharma Expressz Szolgáltató és Kereskedelmi Kft contra Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet.

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• Pharma Expressz Szolgáltató és Kereskedelmi Kft contra Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet.

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• Criminal proceedings against Christina Bellamy and English Shop Wholesale SA, party liable at civil law.
• Staat der Nederlanden v Antroposana, Patiëntenvereniging voor Antroposofische Gezondheidszorg and Others.
• European Commission v Republic of Poland.
• Novartis Pharma GmbH v Apozyt GmbH.
• Ludwigs - Apotheke München Internationale Apotheke v Juers Pharma Import-Export GmbH.



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• VIPA Kereskedelmi és Szolgáltató Kft. v Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet.
• Deutscher Apothekerverband eV v 0800 DocMorris NV and Jacques Waterval.
• 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 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 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
• Directive 98/34/EC of the European Parliament and of the Council of 22 June 1998 laying down a procedure for the provision of information in the field of technical standards and regulations
• Directive 98/48/EC of the European Parliament and of the Council of 20 July 1998 amending Directive 98/34/EC laying down a procedure for the provision of information in the field of technical standards and regulations
• Consolidated version of the Treaty on the Functioning of the European Union 2016/C 202/01
• 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)
• Commission Regulation (EC) No 44/2004 of 9 January 2004 concerning tenders submitted in response to the invitation to tender for the export of husked long grain B rice to the island of Réunion referred to in Regulation (EC) No 1878/2003
• Directive 2012/26/EU of the European Parliament and of the Council of 25 October 2012 amending Directive 2001/83/EC as regards pharmacovigilance Text with EEA relevance