Single Institutional Review Board

Streamline the transition from protocol submission to site activation by providing parallel approvals across all participating institutions.

Ensure absolute consistency in the protection of human subjects by applying a single, high-standard ethical framework to all research activities, regardless of geography.

Centralize and manage complex institutional relationships through established platforms like SMART IRB, reducing the legal and administrative overhead for individual sites.

Coordinate professional translation services for Informed Consent Forms (ICFs) and study materials, ensuring compliance and clarity for diverse, non-English speaking populations.

Serve as the primary point of contact for all IRB-related reporting, including amendments, renewals, and unanticipated problems, allowing study teams to focus on science over paperwork.

Reducing the risk of protocol drift where different local ethical review boards might request conflicting changes to a study design.