Forms and Guidelines

All initial REB applications can be submitted using the eREB system. Review the list of required documents that should be included with an initial REB application submission.

For studies requiring full board review, the complete application package must be submitted at least two weeks prior to a REB meeting date.

Initial submissions

Forms	Guidelines
Case report template Informed consent form template - clinical trials Informed consent form template - minimal risk studies Registry consent form template Verbal consent form checklist	Guideline for determining if a study is research or quality improvement Guideline on accessing shared systems for patients involved in clinical trials Informed consent checklist Guidelines for recruitment material Guidelines for email communication in research Guidelines for remote consent process
Protocol template Master linking log template Interview guide template

Ongoing submissions

Forms	Guidelines
Amendment form Change in study personnel form
Annual renewal/study closure form
Protocol deviation report form	Guideline for reporting protocol deviations
Internal serious adverse event/unanticipated problem report form External serious adverse event/unanticipated problem report form	Guidelines for reporting serious adverse events/unanticipated problems

Forms and Guidelines

Initial submissions

Ongoing submissions

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