CDE integrates siloed trial subject data from multiple systems (EDC, labs, IVR, ECG) into a standardized structure. It automates mapping, harmonization, and downstream sharing to reduce manual entry, errors, and latency. With 1,750+ active integrations and 70 specialists, it supports CTMS, payments, analytics, and risk-based quality management. Benefits include consistent subject records, automated workflows, cost savings, and stronger compliance through full documentation and traceability.

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