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The European Medicine Agency's (EMA) linguistic policy with regard to the submission of information on medicinal products, pursuant to Article 57(2) of Regulation 726/2004

The European Medicine Agency's (EMA) linguistic policy with regard to the submission of information on medicinal products, pursuant to Article 57(2) of Regulation 726/2004[1].



[1] Regulation (EC) No 726/2004 of the European Parliament and of the Council laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, OJ L 136, p. 1