Clinical

SURAI provides a study-centered workspace for coordinating operational context, expected documentation, trial records, responsibilities, and follow-up across studies, countries, and sites.

• Establish a shared study context

  Bring study structure, countries, sites, milestones, documents, and related work into a connected operational view.

• Plan documentation expectations

  Define expected document requirements, applicability, ownership, and target dates using the relevant study, country, or site context.

• Maintain organized and traceable documentation

  Connect documents with their expected requirements and preserve their relationship to the study structure and supporting records.

• Focus attention on gaps and follow-up

  Review completeness indicators, missing documentation, assigned tasks, and review progress to identify work requiring attention.

• Use AI with human oversight

  Ask SURAI to find and summarize study information, help identify documentation gaps, and provide context-aware assistance while keeping review and decisions with authorized users.

• Keep supporting work connected

  Link role-based access, document versions, tasks, notifications, and audit history to the study activities and records they support.

Together, these capabilities help clinical teams coordinate study operations and documentation with greater visibility, context, and control.