WORKFLOW EVALUATION — NOT FOR PATIENT CARE. AI is research-only. No identifiable data without signed agreements.
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EchoReview supports cardiologist review and documented sign-off. AI is in development, research-only, and must not guide diagnosis, treatment, urgency, or routing. Routine uploads and reporting exclude experimental AI. Separate research benchmarks remain available to administrators. Hospital use requires an approved data flow; do not upload identifiable patient data without required agreements and verified provider coverage.

Evaluation scope and commercial terms

Agree scope before pricing

Start with a workflow demonstration or discuss a non-clinical retrospective / shadow evaluation. Duration, study count, staffing, fees, and support require an approved written proposal; no free pilot, fixed per-study rate, or refund is promised here.

Define what the proposal includes

Specify permitted study delivery, available views and clips, reviewer accounts, cardiologist review, documented sign-off, and export requirements. Connector configuration and hospital acceptance testing must be scoped separately. No HL7 / RIS integration, dedicated reading panel, 24/7 coverage, or service-level guarantee is asserted.

Reader services are not assumed

The review platform does not by itself provide cardiologist staffing, licensure, hospital credentialing, clinical insurance, or clinical deployment approval. Agree those responsibilities and any reading-service fees separately.

Measure economics without assumed gains

Record your actual volume, handoff and review times, staffing costs, missing-study work, and proposed fees. Compare measured evaluation results with the site baseline. No four-hour turnaround, additional-volume percentage, cost saving, or revenue increase has been established.

AI is not part of the commercial offer

AI is in development and research-only, not a reading, grading, measurement, or triage service. Routine uploads, connector deliveries, and cardiologist reporting exclude experimental AI. Hospital approval and privacy checks remain required before a patient-data pilot.