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)
• 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)

Billing Information

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