EDC encompasses a full range of clinical data management activities including easy eCRF design build, study setup, edit check creation, and query management.

CIMS offers robust EDC encompassing a full range of clinical data management activities including: eCRF design build, study setup, edit check creation, comprehensive query management, flexibly adding unscheduled forms, and efficient source document verification (SDV). CIMS’ EDC is natively integrated with the eClinical Suite providing full software support for your clinical trial.

Clinical databases and edit checks can be built quickly with an efficient workflow.

• The status bars, with unique two-dimensional features, allow for easy drill-down to each data point.

• The built-in query management system addresses query release and resolution, providing a comprehensive audit trail.

• Optimized for use on any device.

The system can be configured for either 100% Source Data Verification (SDV) or risk-based monitoring based on a predefined risk score.

The EDC can integrate with other CIMS products (RTMS, eSafety, Encoder, and DDM™) to support and streamline comprehensive studies, enhancing data collection, integrity, and traceability.

The EDC is equipped with various customized reports, including progress reports by center or investigator, query status reports, adverse event (AE) reports, individual Subject profiles, and population-based data displays.

CIMS’ offers a unique, built-in SDTM mapper that maps and creates SDTM databases with annotated CRFs, as well as define files.

Schedule a demo with us to learn about EDC and how it can benefit your organization.

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