A principal investigator shall ensure compliance of a clinical trial at a clinical trial site with the requirements of this Regulation.
The principal investigator shall assign tasks among the members of the team of investigators in a way which is not compromising the safety of subjects and the reliability and robustness of the data generated in the clinical trial at that clinical trial site.
Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04
CitationArticle 73 of Regulation (EU) No 536/2014 (LawPlayer, data as of 2026-07-04)