The Integrated Research Information System (iRIS) is an electronic research administration platform used to manage protocol submissions, review workflows, approvals, and regulatory documentation.
iRIS centralizes investigator submissions, routes materials for committee review, and maintains structured records such as reviewer comments, determinations, and approval history. Features like version control, audit trails, and role-based access support traceability and compliant recordkeeping. In clinical research, iRIS improves operational visibility by enabling teams to track status, manage amendments, and maintain documentation consistency. Standardized workflow systems reduce administrative errors and support efficient oversight of human research protections.