Image analysis
Segmentation and detection across MRI, CT, X-ray and digital pathology. Every finding traces back to the voxels that produced it.
Bedside pre-reads every study and every new observation, ranks what needs a clinician now, and shows the evidence behind each flag. A clinician signs every report.
Each figure below is footnoted with its method and links to an auditable model card.
Every model ships with its own evaluation set, a drift monitor and a plain-language explanation for the clinician reading it.
Segmentation and detection across MRI, CT, X-ray and digital pathology. Every finding traces back to the voxels that produced it.
Deterioration, sepsis and readmission risk, recalculated on every new observation instead of once a shift.
Options ranked against the patient's own history, comorbidities and genomic signals, with the trade-offs shown.
Build a de-identified cohort from a plain-language query and export it to your notebook with provenance intact.
Scores recompute on every observation. Pick a cohort to see the last 12 hours and where the alert threshold sits.
Sepsis · 6 h median lead time before the first vital sign crosses its limit.
Rising lactate, HR +18 over 4 h, falling urine output. Escalate per sepsis pathway.
Weight up 1.8 kg in 3 days with SpO₂ drift. Review diuretic dose.
Stable across all tracked signals. Next recompute in 15 min.
No new window to learn. Results land in the PACS worklist and the chart your team already opens.
Point your PACS and HL7 or FHIR feed at an endpoint in your own VPC. Data stays in your region, and nothing trains on it without a signed addendum.
Run in shadow mode. Compare model output with your own reads, then set alert thresholds for each service line.
Findings arrive as a pre-read with the evidence attached. Drift monitors and a weekly model card keep your governance board current.
“The value wasn’t replacing a read. It was knowing which twelve studies to open first.”
Everything a clinical safety officer asks for on day one, available before you talk to sales.
Anything not covered here goes to our clinical safety lead, who replies within one working day.
Ask a questionNo. It produces a pre-read with confidence scores and the evidence behind them. A clinician reviews and signs every report, and every override is logged and added to the evaluation set.
In your region, in a VPC you control. De-identification happens before anything leaves that perimeter, and no customer data is used for training without a signed addendum naming the exact cohort.
Two weeks to a shadow-mode deployment for a typical PACS and HL7 feed. Then four weeks of calibration against your own reads before anything reaches a clinician.
Misses and false positives are reviewed weekly with your clinical safety officer. Thresholds can be tuned per service line, and any model version can be rolled back from the console.
Drift monitors compare live inputs and outputs with the validation set every week. A drop past the agreed limit alerts your safety officer and pauses that model's flags until it is reviewed.
Start with one service line and a four-week shadow deployment. If the numbers don’t hold up against your own reads, you walk away.