[117: 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 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Consolidated version: 05/06/2013).
[117: Eiropas Parlamenta un Padomes 2001. gada 6. novembra Direktīva 2001/83/EK par Kopienas kodeksu, kas attiecas uz cilvēkiem paredzētām zālēm; Eiropas Parlamenta un Padomes 2004. gada 31. marta Regula (EK)