Clinical Trials Committee  |  Templates and Forms

Placebo Controlled Trials 

Justification for Placebo Controlled Trials – Guidance document

Reportable Events 

For specific criteria, and links to forms, please go to this page.

Consent Forms

• Consent to Disclose Health Registration Information Template  (updated 19 August 2021)
• Informed Consent Template for Standard Research Studies
• Genetic Informed Consent Form Template
• Caregiver Participation Form

Checklists

• Reviewer Form
• Checklists for Submission of a Research Study

Reviews and Study Requirements

• Items Required For Review
• Board of Record Agreement for investigators conducting research through private practice or other community-based organizations (both for and not-for profit).  For investigators who conduct their research under the auspices of either Alberta Health Services, Covenant Health, Universities of Alberta or Calgary, the 2016 Research Ethics Reciprocity Agreement(amended May 31, 2021) will act as this agreement – no action is required.  If you do not have a fully executed BOR on file with HREBA, please complete the BOR Information Form at the bottom of the linked page and send to info@hreba.ca.

Billing Information

If your study is industry funded, please submit a HREBA Billing Information Form  (Revised)
Upload the completed Billing Information Form to the “REB Service(s) Fee” section in IRISS.