EURegulation (EC) No 141/2000 of the European Parliament and of the Council of 16 December 1999 on orphan medicinal products
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EUCommission Regulation (EC) No 847/2000 of 27 April 2000 laying down the provisions for implementation of the criteria for designation of a medicinal product as an orphan medicinal product and definitions of the concepts 'similar medicinal product' and 'clinical superiority'
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EUCheminova A/S and Others v Commission of the European Communities (T-326/07)
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EUMylan IRE Healthcare Ltd v European Commission (T-303/16)
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EUBristol-Myers Squibb Pharma EEIG v European Commission and European Medicines Agency (T-329/16)
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EUCouncil 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
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EUPharma Mar, SA v European Commission (T-594/18)
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EUShire Pharmaceuticals Ireland Ltd v European Medicines Agency (T-80/16)