MONTRÉAL
Clinical Trial Monitoring Methodology,
Site Management and Coordination
Systematic Approach to Effectively Monitor Multi-Center Clinical Trials
Safety and SAE Reporting,
Principals of data management and query resolution
ICH GCP (E6, E2), 21 CFR 50, 54, 56, 312, FDA 1572, 45 CFR 46, FRSQ Regulation. Knowledge of clinical study and medical terminology
