[19: 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, http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:L:2001:311:0067:0128:en:PDF ][20: Regulation 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, https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-1/reg_2004_726/reg_2004_726_en.pdf ]
[19: Eiropas Parlamenta un Padomes 2001. gada 6. novembra Direktīva 2001/83/EK par Kopienas kodeksu, kas attiecas uz cilvēkiem paredzētām zālēm, http://eur-lex.europa.eu/legal-content/LV/TXT/PDF/?uri=CELEX:32001L0083&qid=1526033757837&from=EN ][20: Eiropas Parlamenta un padomes Regula (EK) Nr. 726/2004 (2004. gada 31. marts), ar ko nosaka cilvēkiem paredzēto un veterināro zāļu reģistrēšanas un uzraudzības Kopienas procedūras un izveido Eiropas Zāļu aģentūru, https://ec.europa.eu/health/sites/health/files/files/eudralex/vol-1/reg_2004_726/reg_2004_726_lv.pdf ]