Adverse Event Reporting Form - Mar 2022

The Adverse Event Reporting Form is used by researchers to report any adverse events that occur during a clinical trial. The form requires the researcher to provide information such as the participant's name, the nature of the event, the severity of the event, and any medical treatment provided.

Researchers conducting clinical trials in Canada should complete the report.

The completed Adverse Event Reporting form should be submitted to the Research Ethics Board responsible for the clinical trial.