Clinical Trials Committee | Templates and Forms
Placebo Controlled Trials
For specific criteria, and links to forms, please go to this page.
- Consent to Disclose Health Registration Information Template
- Informed Consent Template for Standard Research Studies
- Genetic Informed Consent Form Template
- Caregiver Participation Form
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)
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.