(161) Za potrebe pristanka za sudjelovanje u aktivnostima znanstvenog istraživanja u okviru kliničkih ispitivanja trebale bi se primjenjivati relevantne odredbe Uredbe (EU) br.
536/2014 Europskog parlamenta i Vijeća (15).
(161) For the purpose of consenting to the participation in scientific research activities in clinical trials, the relevant provisions of Regulation (EU) No 536/2014 of the European Parliament and of the Council [15] should apply.
(15) Uredba (EU) br. 536/2014 Europskog parlamenta i Vijeća od 16. travnja 2014. o kliničkim ispitivanjima lijekova za primjenu kod ljudi te o stavljanju izvan snage Direktive 2001/20/EZ (SL L 158, 27.5.2014., str. 1.). https://eur-lex.europa.eu/legal-content/EN/AUTO/?uri=OJ:L:2014:158:TOC
[15] Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC (OJ L 158, 27.5.2014, p. 1). https://eur-lex.europa.eu/legal-content/EN/AUTO/?uri=OJ:L:2014:158:TOC
The latest consolidated version of the Regulation with corrections by Corrigendum, OJ L 127, 23.5.2018, p. 2 ((EU) 2016/679). Source: EUR-lex.