Aggregate, reconcile, and validate encounter and risk data across RAPS, EDPS, 837 submissions, and internal systems for completeness and compliance.
Automate submission workflows with built-in validation, error resolution, and status tracking to ensure timely, compliant reporting.
Generate CMS-aligned RADV evidence packs with full source documentation and clinical traceability.
Conduct mock audits and checks to validate diagnoses with explainable AI, workflows, and human oversight.
Maintain continuous audit readiness with full transparency and defensible documentation from source to CMS submission.