Worklist
Prioritize studies by urgency, due-time, and site rules. The right case surfaces next.
For Radiology Groups & Imaging Centers
Worklist. Viewer. Reporting. Compliance. A single platform that replaces fragmented tools and keeps your team inspection-ready.
| Patient | MRN | Study | Modality | Priority | Status |
|---|---|---|---|---|---|
| Martinez, Elena R | MRN-4821 | Dx Mammo Bilateral | MG | Urgent | Reading |
| Chen, Margaret L | MRN-7193 | Dx Mammo Left | MG | Routine | Queued |
| Thompson, Sarah K | MRN-3567 | Screening Mammo | MG | Routine | Queued |
| Davis, Patricia A | MRN-9284 | Dx Mammo Bilateral | MG | Urgent | Queued |
| Wilson, Janet M | MRN-6130 | Screening Mammo | MG | Routine | Complete |
Unified Worklist + Viewer + Reporting
MQSA & FDA Inspection-Ready
Multi-Site Ready
The Problem
Disconnected worklist, PACS, viewer, and reporting systems create delays, increase rework, and make inspection prep reactive instead of routine.
Platform
Prioritize studies by urgency, due-time, and site rules. The right case surfaces next.
Optimized storage and retrieval with fast study access built for breast imaging.
Tuned for mammography read patterns, comparison workflows, and hanging protocols.
Templates with consistency controls that reduce variability and rework.
Centralized evidence trails and policy-linked workflows for MQSA/FDA readiness.
Finalized reports sync downstream with traceable status across systems.
Voice-assisted reporting reduces typing burden during reads.
Prior reports and intake context surfaced in one view before interpretation.
Consistent educational materials aligned to each stage of the patient journey.
Reference atlas for faster, more consistent complex interpretations.
Outcomes
Workflow
Step 1
Prior exams, intake data, and clinical history in one summary before you start.
Full context before every read.
Step 2
Read in a breast-focused viewer. Draft structured reports with voice support.
Guided interpretation, consistent output.
Step 3
Finalize and sync results into RIS-PACS with traceable status.
Reliable delivery across your stack.
Compliance
Centralize policy-linked artifacts and reduce last-minute audit prep overhead across every site.
Maintain evidence trails for MQSA and FDA inspections.
Link reports, documentation, and procedural records.
Structured operational checkpoints replace last-minute prep.
Repeatable compliance steps across every site.
Supports inspection-readiness workflows and documentation discipline. Does not replace legal, clinical, or regulatory governance obligations.
FAQ
No. Rollout is staged around your existing stack and highest-impact bottlenecks first.
No. The platform supports centers across different volumes and maturity levels.
Yes. Most teams start with worklist, viewer, and reporting before expanding.
We use a phased readiness plan to establish baseline documentation workflows first.
Get Started
Share your organization, monthly volume, and current RIS/PACS setup. We tailor every demo to your environment.
Email goes directly to our intake team.
Include your workflow details for a tailored demo.
intake@example.com
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