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

  • Currently under development


Informed Consent Forms


Clinical Trial Application to Health Canada

Drug Development

Electronic Data Capture and Data Management/Analysis
Budget Development


Agreements


Data Safety Monitoring Board

  • Currently under development


Quality Assurance/ Clinical Monitoring

  • MICYRN has recently become a member of N2 (Network of Networks) and has access to tools and resources for best practices in clinical research including Health Canada approved standard operating procedures. For more information regarding SOPs and ICH-GCP training certifications please contact Breanne Stewart.


Ethics Application/Approval

  • Ethics Harmonization Process (forthcoming)

Operational Approvals

  • Currently under development


Lab Considerations
Trial Registration
Document and Data Archiving


Patient Engagement


Knowledge Translation


CONSORT

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

View checklist here


Research Resources


Biobanking