REMINDER: The Research Ethics Office is not accepting hard copy submissions. Submissions for pre-eREB studies should sent to the REB Inbox (email@example.com). Send only one form (with related attachments) per email. All communications to the REB Inbox should be sent by the PI or by a research team member with the PI cc’d.
NOTE: Please check that the version date of the document that you download matches the version date on this page. If you are getting an earlier version of the file, please clear the cached files from your browser and try downloading again.
|FOR NEW APPLICATIONS|
|Applications for new studies must be submitted through the Unity Health eREB.|
|For submissions through CTO (Clinical Trials Ontario) studies, please see:|
Clinical Trials Ontario (CTO) at Unity Health
|FOR SUBMISSIONS RELATED TO APPROVED STUDIES|
|Amendment request form||August 18, 2021|
|Continuing review form (Full Board) |
Use this form only if the study is FDA regulated or US federally funded and has had active participants in the past year.
|March 31, 2021|
|Continuing review form (Delegated)|
Most studies can use this form to request annual review of their research,
The only studies that cannot use this form are those that are FDA regulated or US federally funded and have had active participants in the past year.
|April 07, 2021|
|External serious adverse events / unanticipated problem reporting form||November 01, 2019|
|Local serious adverse events / unanticipated problem reporting form||November 01, 2019|
|Protocol deviation reporting form||November 01, 2019|
|Staff change form||March, 01, 2022|
|Study closure form||May 17, 2022|
|Updated safety information reporting form||November 01, 2019|