The following materials are required for review:
- Protocol
- Copy of the Investigational Drug Brochure/Product Monograph (if applicable)
- Electronic copy of the Consent Form (must provide an electronic copy in Word format)
- Copy of Curriculum Vitae and Copy of Current Medical License (for Principal Investigators only)
- Completed Site Questionnaire (for each Principal Investigator) (see below)
Following are links to PDF downloads to aid in preparing a submission:
- 2023 Submission Checklist PDF format
Save PDF File - 2023 Site Questionnaire PDF format
Save PDF File - 2023 Submission Guide PDF for further information about the submission process/continuing review/information about our Board
Save PDF File