Castor

Castor combines EDC, eConsent, eCOA, and real-world evidence workflows in a cloud-native platform with a shared data layer. Its services team also supports study builds, data management, eCOA delivery, and regulated translation.

Clinical Trial Data Capture

• Capture trial data with Castor EDC, using validated eCRFs and a shared data layer for collection and management.
• Collect patient-, observer-, and clinician-reported outcomes through managed eCOA/ePRO workflows, including BYOD and provisioned devices.

Data Management and Submission

• Manage validation, queries, reconciliation, SDTM alignment, and database lock in Castor CDMS without moving data between systems.
• Prepare regulatory exports with validated datasets and Define.xml generation for FDA, EMA, and PMDA submission workflows.

Evidence and Remote Operations

• Collect structured data for registries, observational studies, chart reviews, and post-market evidence programs, with audit trails.
• Support remote and hybrid studies with eConsent, eRecruitment, participant communications, remote monitoring, and source-data extraction with human review.

Best Fit

• Sponsors, CROs, investigators, and research sites needing one platform for clinical data capture, outcome collection, and data management.
• Medical device teams can support EU MDR PMCF studies with registry, survey, and chart-review designs, structured exports, and audit trails.