Reducing duplication of efforts through shared resources.
Multi-Site Clinical Trial Checklist
Protocol Development
SPIRIT Protocol
Biostatistical Support
Currently under development
Informed Consent Forms
Assent Template 1
Assent Template 2 — Clinical Research
Adolescent Assent Template
Deferred Consent — Clinical Research (Resource)
Deferred Consent — Drug Trials (Resource)
Clinical Trial Application to Health Canada
CTA Application
Good Clinical Practice Guidance
ITA Application
Drug Development
Bay Area Research Logistics—Placebo Templates
Placebo Development
Pharmacology Working Group Service (in development)
Electronic Data Capture, Budget Development, and Data Management and Analysis
Currently under development.
Agreements
MICYRN Lawyer Network
Study Terms of Reference Checklist
Data Safety Monitoring Board
Currently under development.
Quality Assurance and Clinical Monitoring
MICYRN is 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 and Approval
Ethics Harmonization Process (forthcoming)
Operational Approvals
Currently under development.
Lab Considerations
Currently under development.
Trial Registration
Currently under development.
Document and Data Archiving
Currently under development.
Patient Engagement
CIHR Patient Engagement Materials
Knowledge Translation
Currently under development.
CONSORT
The CONSORT - Transparent Reporting of Trials website provides a checklist to ensure proper trial reporting.
Biobanking Resources
Anything missing? Please contact us!