This page provides a quick link to Bannatyne Campus Research Ethics Boards Templates and should only be accessed following the review of web pages on this site relating to initial and continuing review Submission Requirements.
NOTE: All requests for review (including requests for delegated review) of new projects must be submitted to the Bannatyne Campus Research Ethics Board office by the monthly full board meeting deadline dates.
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New Studies/Initial Review Checklists
New Studies/Initial Review Submission Forms
Annual Approval Checklists
Amendments and/or Changes Checklists
Adverse Event Reporting and Safety Data Forms
Protocol Deviation Reports
Template/Tools for Research Sites
Request for Preliminary Access
During COVID-19 email submissions are required. Paper copies will not be accepted by the office. Please consider this when reviewing the checklist of requirements. Review Submission Requirements.
Checklist for Full Board Review of New Studies (pdf)
Checklist for Delegated Review of New Studies (pdf)
Checklist for Single Case Report (pdf)
Human Research Review Sub-Committee Research Proposal Summary (docx)
Informed Consent Form Template for Clinical Trials (doc)
Non-Clinical Trial Informed Consent Form Template for Non-Clinical Trials (doc)
Assent Template (doc)
Focus Group or Individual Interview Consent Template (doc)
Basic Elements of Consent Disclosure Statements for Survey Research (docx)
Informed Consent Form Template for Permission to be contacted for Future Research (docx)
Local Adverse Event Unanticipated Problems Form (Initial) (pdf)| Instructions
Local Adverse Event Unanticipated Problems (Follow up) (pdf)
External (Non Local) Adverse Event Form (pdf) | Instructions
Updated Safety Information Form (pdf) | Instructions
Periodic Safety Update Form (pdf) Instructions
P.I. Curriculum Vitae Template - ONE per year only (pdf)
Sample Data Capture Sheet (docx)
Sample Master List for Data Capture Lists (docx)
Questionnaire Appendix Cover Page (docx)
Recruitment/Social Media Appendix Cover Page (docx)
Diaries, Patient Contact Cards and Retention Items (docx)
RPA Form (pdf)
RPA Amendment Form (pdf)
Review the Researcher Training Manual
Review the Common Submission Pitfalls brochure
TIPS FOR SUBMITTING CONSENT FORMS READ TEMPLATE INSTRUCTIONS PAGE PRIOR TO USING.
Use simple language and avoid medical jargon.
Check for spelling, typing and grammatical errors prior to submitting.
Review consent forms to ensure only applicable wording is included in version submitted to REB.
The BOLDING and UNDERLINING that appears in the ICF templates is for ease of use only. Please remember to remove the Bolding and Underlining from the Informed Consent Forms before submitting them.
Insert a version date in the footer of each page and change when revisions are made.
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