Forms and Guidelines

Initial submissions

REB Application for Prospective Studies (TAHSN) (DOC)

REB Application for Retrospective Access to Health Records (DOC)

REB Application for Use of Tissue/Blood/Body Fluid (DOC)

Sample Consent Template (DOC)

Consent Form Summary (DOC)

Ongoing submissions

Amendment/Administrative Change Form (DOC)

Change in Study Personnel Form (DOC)

Annual Renewal/Termination Report Form (DOC)

Protocol Deviation Report Form (DOC)

External SAE/Unanticipated Problem Report Form (DOC)

Internal SAE/Unanticipated Problem Report Form (DOC)

Guidelines for REB Application for Prospective Studies (TAHSN) (DOC)

Guidelines for writing proposals and consent forms (DOC)

Guidelines for recruitment materials (DOC)

Guidelines for Amendments/Administrative Changes (DOC)

Guidelines on Annual Renewals (DOC)

Guidelines on Study Completion (DOC)

Guidelines for Reporting Protocol Deviations (DOC)

Guidelines for Reporting SAEs/Unanticipated Problems (DOC)

When constructing a consent form, please choose the Confidentiality section that best fits your study type:  

Sponsored, Health Canada registered study (DOC)

Sponsored study, not registered with Health Canada (DOC)

Non-sponsored, Health Canada registered, multi-site study (DOC)

Non-sponsored, Health Canada registered, MSH-only study (DOC)

Non-sponsored, multi-site study, not registered with Health Canada (DOC)

Non-sponsored, MSH-only study, not registered with Health Canada  (DOC)