Import and triage all CTMS, spreadsheet, and SAS data into study forms.
Automatically assess your portfolio against regulatory requirements. Study-level controls let you manage auto-assessment, surface missing fields needed for calculation, and handle recurring assessments.
Streamline data entry with a configurable primary form and enable or disable registry views according to your disclosure strategy. Intelligently sync data across registries preserving registry-specific values where needed.
Manage transparency activities with intuitive project tracking, dashboards, and detailed reports.
Streamline collaboration with improved mention and review/approval workflows, making it easier to coordinate across reviewer and approver roles.
Seamlessly submit trial data directly to registries or with downloadable XML file with full visibility and a streamlined handoff from authoring to submission.
