Downloadable Application Forms
Submission & Application Process
Required Submission Materials
To submit a protocol for IRB review:
1. Application Form: Completed and signed by the Principal Investigator (PI) and/or the Scientific Department Chairperson.
2. Consent Forms: English or Arabic consent forms (unless requesting a formal waiver).
3. Research Instruments: Final surveys, questionnaires, tests, or interview guides (for pilot studies, submit representative drafts).
4. Recruitment Materials: Advertisements, flyers, brochures, or letters intended for prospective participants.
5. Investigator Documentation: CVs of the PI and co-investigators (Include Clinical Investigator Brochure, Insurance Certificate, or Clinical Trial Agreement if applicable).