Recital 161

Consent in Clinical Trials Unofficial title

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.

Footnotes

(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://gdpr.digiphile.law/recital/recital-161.html

Text as at 19 September 2026.

This is an unofficial convenience version of the EU GDPR (Regulation (EU) 2016/679). It is presented “as is” without guarantee of accuracy, completeness or reliability. See the source text for the official version. This site was last updated in September 2026.