To support the design and conduct of clinical trials, the CTO provides a broad suite of tools, templates & resources. Browse the table of contents of available tools & templates below and sign up for free access.
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Interventional Protocol Template
Observational Protocol Template
Qualified Investigator Undertaking (QIU)
Data Safety Monitoring Board (DSMB)
Personnel Training Log
Delegation of Responsibility Log
Adverse Event Log
Pharmacy
Drug Temperature Monitoring
Protocol Violations/Deviations
Subject Visit Tracking Log
Notes-to-File
Adverse Events
Demographics
Inclusion Exclusion Criteria
Medical History I
Medical History II
Physical Exam
Prior and Concomitant Medications
Protocol Deviations
Randomization and Enrollment
Serious Adverse Events
Study Completion
Visit Checklist
Vital Signs
Device Accountability Log
Drug Accountability Log
Investigational Product Subject Compliance Tracking Tool
Master Identification Log
Screening and Enrolment Log
Subject Contact Log
Off Study Form
Close Out Checklist
Sample Health Canada Closure Letter
Participant Contact Log
Patient Follow Up Letter
Subject ID List
Telephone Log
Equipment Calibration Note-to-File
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