Covers the full lifecycle of a human subjects research study — from new submissions and amendments to renewals and closures. This includes investigator-driven proposals, IRB reviews, continuing review management, and decision tracking.
Connects all parties involved — investigators, IRB members, coordinators, and compliance officers — through a unified workspace. Smart workflows, automated reminders, and meeting scheduling help keep reviews on track while reducing administrative burden.
Ensures compliance with federal and institutional requirements, including OHRP, FDA, and NIH regulations. The system supports structured decision-making, detailed audit trails, and policy adherence, reinforcing ethical standards throughout every submission.