Templates for Clinical Trials

Multi-Centre Trials

This checklist is to help sites ensure they have all the requirements for a multi-site clinical trial. Links are continually updated, so please check back for the latest additions.

Protocol Development
Biostatistical Support
Informed Consent Forms

Clinical Trial Application to Health Canada

Drug Development

Electronic Data Capture and Data Management/Analysis
Budget Development
Data Safety Monitoring Board
Quality Assurance/ Clinical Monitoring
Ethics Application/Approval
Operational Approvals
Lab Considerations
Trial Registration
Document and Data Archiving
Patient Engagement
Knowledge Translation


The CONSORT - Transparent Reporting of Trials website provides a checklist to ensure proper trial reporting.

View checklist here

Research Resources