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Procedures
- Research Ethics Committee Procedures (effective February 2011)
- ACREC Full Board Review Process
Application Forms
- Research Ethics Committee Application (effective February 2013)
- Combined Protocol and Minimal Risk Application (effective September 2012)
- Co-Investigator Form (effective September 2012)
- Change of Study Staff Form (effective September 2012)
- Research Ethics Committee IB or PM submission Form (effective September 2012)
- Protocol Deviation Reporting Form (effective September 2012)
- Amendment Submission Template (effective September 2012)
Consent Form Guidance and Templates
- Main Consent Form Template (effective November 2012)
- Banking for Future Research Consent Form Template (effective November 2012)
- Required Elements for Informed Consent Checklist
Annual Renewal Reporting
- Annual Renewal Reporting Guidance (effective September 2012)
- Annual Renewal Form (effective September 2012)
- Study Completion Form (effective September 2012)
- Study Termination Guidance (effective September 2012)
- Study Reactivation Form (effective September 2012)
Serious Adverse Event Reporting
- Non-Local Adverse Event Reporting (effective March 2011)
- SAE Reporting Guidelines (effective September 2012)
- Local SAE Reporting Form (effective September 2012)
- Non-Local SAE Reporting Form (effective September 2012)
Investigator Initiated Research
If a formal protocol is not available for Investigator Initiated Research, the ACREC Minimal Risk Application provides a protocol template which should be used as a guide.
- Protocol Signature Sheet (effective April 2009)
- Subject Enrolment Log (effective April 2009)
- Study Delegation Log and Signature Sheet (effective April 2009)
- Prohibited Medication List Template (effective January 2009)
- Concomitant Medication Sheet (effective April 2009)
