Preferred Label : Clinical Trial Investigator Regulatory Agreement Documentation;
NCIt related terms : Invstgr Reg Agrmnt; Investigator Regulatory Agreement;
Alternative definition : CareLex: A regulatory statement from the investigator required by certain health authorities.
Examples are a Qualified Investigator Undertaking form and Clinical Trial Site Information
form required by Health Canada. [Adapted from TMF-RM]; CDISC: Documentation containing the agreement by any/all investigators of the clinical
trial that all trial activities will conform fully to all regulations as set forth
by the law, or any other supervisory authority.;
Origin ID : C115477;
UMLS CUI : C3899581;
Semantic type(s)
- concept_is_in_subset
