AuraOne
Domain Lab

The patient comes first. The proof comes with it.
Auditable. Defensible. Regulator-ready. AI reads every study. Specialists verify the findings.
For clinical AI teams where a missed finding is a patient safety event.

Ingest DICOM studies and WSI slides. AI runs diagnostic classification, tumor segmentation, and biomarker scoring. Results ship with FDA 510(k)/HIPAA evidence packs.

Your first run

10 DICOM studies. Structured findings and specialist review. First evidence pack in days.

AI LabsTrustScore™ WorkforceControl Center
Accepted formats
DICOM / WSI / NIfTI

Ingest imaging studies and whole-slide images from your PACS or scanner.

Compliance frameworks
FDA 510(k) / HIPAA

Evidence packs structured for FDA submission and HIPAA compliance.

Pre-built agent
diagnostic-classifier

Diagnostic classification, tumor segmentation, and biomarker scoring.

Focus Areas

What this lab is built for.

Surfaces designed for scientists, operators, and executives. Every output is versioned with provenance so no work is lost.

Diagnostic Imaging

Structured, reviewable outputs.

  • Generate overlays and structured findings from DICOM studies
  • Route uncertain cases to calibrated specialist reviewers
  • Tumor segmentation and treatment response assessment for oncology
  • Keep provenance attached to every correction and decision

Biomarker Scoring

Quantified precision.

  • Biomarker scoring workflows calibrated to your program
  • Structured reviewer corrections and adjudication trails
  • Consistent measurement with provenance capture

Specialist Loop

Expert calibration and escalation.

  • Review steps designed for specialist clinical workflows
  • Escalation with rationale and full clinical context
  • Versioned outputs for downstream clinical systems
Signature Workflow

How Medical & Oncology runs.

Automated evaluation. Expert routing. Regression-tested releases.

Step 1

Ingest

Bring in imaging data.

  • Ingest DICOM studies, WSI slides, and clinical metadata
  • Validate required fields and program constraints
  • Attach retention and export requirements up front
Step 2

Analyze

Score and classify.

  • Run diagnostic classification and tumor segmentation
  • Generate candidate findings for specialist review
  • Record intermediate evidence and uncertainty signals
Step 3

Report

Review, approve, export.

  • Specialist sign-off or corrections with rationale
  • Escalate exceptions with full clinical context attached
  • Export FDA 510(k)/EU AI Act/HIPAA evidence packs

Overview

Ingest your DICOM studies and WSI slides and get diagnostic classification, tumor segmentation, and biomarker scoring — with specialist review and evidence packs that survive clinical scrutiny. AuraOne Medical turns imaging workflows into a repeatable loop: ingest, analyze, verify, export.

Medical & Oncology capsule

Auditable. Defensible. Regulator-ready. AI reads every study. Specialists verify the findings.

  • Ingest DICOM studies and WSI slides. AI runs diagnostic classification, tumor segmentation, and biomarker scoring. Results ship with FDA 510(k)/HIPAA evidence packs.
  • DICOM / WSI / NIfTI Accepted formats
  • Focus: Diagnostic Imaging
  • Workflow: Ingest

Guided review

The platform generates structured findings and overlays that help specialists focus attention. Review steps and decisions stay auditable. For oncology cases, tumor boundaries, staging assessments, and response classifications follow the same pattern.

Medical & Oncology capsule

Auditable. Defensible. Regulator-ready. AI reads every study. Specialists verify the findings.

  • Ingest DICOM studies and WSI slides. AI runs diagnostic classification, tumor segmentation, and biomarker scoring. Results ship with FDA 510(k)/HIPAA evidence packs.
  • DICOM / WSI / NIfTI Accepted formats
  • Focus: Diagnostic Imaging
  • Workflow: Ingest

Evidence for regulators

Every finding, correction, and sign-off is captured with provenance. Export FDA 510(k), EU AI Act, and HIPAA evidence packs when submission or audit demands it.

Medical & Oncology capsule

Auditable. Defensible. Regulator-ready. AI reads every study. Specialists verify the findings.

  • Ingest DICOM studies and WSI slides. AI runs diagnostic classification, tumor segmentation, and biomarker scoring. Results ship with FDA 510(k)/HIPAA evidence packs.
  • DICOM / WSI / NIfTI Accepted formats
  • Focus: Diagnostic Imaging
  • Workflow: Ingest

Proof hooks

Evidence that stays attached

This is what the system is designed to record for Medical & Oncology workflows. Metrics and outcomes depend on your deployment and must be validated in staging and production.

FDA 510(k) / HIPAA
Evidence packs structured for FDA submission and HIPAA compliance.
Specialist trails
Who reviewed what, when, and why — with full clinical context.
EU AI Act
Evidence exports structured for European AI regulatory review.
Want the security and evidence model? Start in the Trust Center.
Visit Trust Center

Start your Medical & Oncology Lab.

One session. First lab running.