Centralized setup, configuration, versioning, and governance of clinical studies from initiation to closure.
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Define study protocols, treatment arms, visit schedules, and operational parameters in a centralized, version-controlled environment.
Configure system-wide settings for notifications, medical dictionaries, and user roles on a per-study basis.
Manage multiple versions of a study build, ensuring a smooth transition for protocol amendments with full audit trails.
Link studies to specific customers (Sponsors/CROs), ensuring strict data segregation and controlled user access.
Operate studies in 'Live' mode for real data or 'Training' mode for UAT and user education, with clear data separation.
Export comprehensive study metadata and configuration details into readable formats for documentation and archival.
Conclusion
Establishes a centralized, authoritative source for all study-related configurations, ensuring consistency.