I imagine what I want to write in my case, I write it in the search engine and I get exactly what I wanted. Thank you!
Valentina R., lawyer
(2014/C 448/11)
Language of the case: Italian
Applicants: Agenzia Italiana del Farmaco (AIFA), Ministry for Health
Defendant: Doc Generici srl
1.Must Article 3(2)(a) of Council Regulation (EC) No 297/95 of 10 February 1995, in the version currently in force, be interpreted as meaning that Type I marketing authorisation variations — and, in particular, in respect of the case in the main proceedings, Type IA variations — where an identical variation affecting several authorisations belonging to the same holder are concerned, are subject to a single fee, to the extent specified therein, or to as many fees as there are authorisations affected by the variation?
2.In the circumstances in the present proceedings, may or must, as held by this Chamber, the question be referred to the Court of Justice?
Council Regulation (EC) No 297/95 of 10 February 1995 on fees payable to the European Agency for the Evaluation of Medicinal Products (OJ 1995 L 35, 15.2.1995, p. 1).
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