Reviewing items for self-report of adverse events in clinical trials
Research type
Research Study
Full title
Reviewing the validity of items for patients to self-report adverse events in clinical trials: A patient cognitive interview study (REPORT-UK Phase 1)
IRAS ID
116109
Contact name
Galina Velikova
Contact email
REC name
Yorkshire & The Humber - Leeds East Research Ethics Committee
REC reference
12/YH/0531
Date of REC Opinion
11 Dec 2012
REC opinion
Favourable Opinion