AI that triages patient-safety risk, writes clinical notes, and shrinks the support ticket volume.

We help US EHR vendors and HealthTech companies turn the clinical, claims, and product data they already own into production AI – governed and HIPAA-safe by default, so it clears security and compliance review.

Book a free data-readiness assessment

30 Minutes | No Commitment | Led by our Healthcare AI Team

GOVERNED FOR

WHAT WE’VE SHIPPED
Real systems, running in HealthTech

Each is built on a governed data foundation and validated by human oversight before it reaches production.

Patient-safety ticket triage

Reportable patient-safety issues are only about 2% of all support tickets — the rest is routine noise like password resets. We built an ML classifier that reads the clinical context of every ticket and isolates that critical 2% automatically, so nothing reportable slips past a tired reviewer.

Ambient AI medical scribe

Clinicians lose up to two hours of documentation for every hour of care. Built on clinical LLMs, our ambient scribe listens to the natural consultation, separates speakers, and writes a structured SOAP note straight into the EHR — no dictation syntax, no human scribe in the room.

GenAI support deflection

EHR platforms are complex, so users skip the docs and file a ticket. Our GenAI engine intercepts the ticket as it’s drafted, answers it from the vendor’s own manuals, and deep-links to the exact timestamped video segment — resolving it before it ever reaches a human agent.

Knowledge-graph clinical decision engine

Hormone optimization needs precise, individualized protocols where a wrong dosage carries real risk. We fused a deterministic knowledge graph with a multi-agent framework: rules select the protocol, a safety agent checks contraindications, and the LLM only writes the patient-friendly summary — collapsing drafting from hours to seconds with hallucination engineered out.

WHAT WE BUILD
Governed AI capabilities for HealthTech

Patient-safety triage

Classify reportable issues out of routine ticket noise using clinical context.

Ambient documentation

Structured SOAP notes generated from natural conversation, into the EHR.

GenAI support deflection

Resolve tier-1 support at ticket creation with answers and video chunks.

Clinical decision engines

Knowledge-graph, multi-agent protocols with safety guardrails – no hallucinated dosages.

Governed data foundation

Clinical, claims, and product data structured with PHI safeguards and lineage.

HITL + audit trails

Human checkpoints and full traceability on every decision, by default.

WHY IT STALLS

HealthTech AI rarely dies on the model.

It dies on the data.

The highest-value signal lives in clinical notes, tickets, and claims – locked behind compliance risk. A governed data foundation engineered for PHI is what lets the work above actually ship. That’s where we start.

the value is

Trapped in the EHR, behind compliance risk.

the blocker is

Ungoverned AI on PHI – so nothing ships.

the unlock is

A governed foundation, built for PHI first.
4

capabilities shipped across EHR & clinical workflows

100%

audit-traceable – a trail on every decision

Weeks

to a governed proof of concept, not quarters

QUICK ANSWERS

The questions buyers actually ask

Will this clear our security and compliance review?

Yes – it’s built to. PHI is encrypted, access-controlled, and logged; a Business Associate Agreement (BAA) is in place; humans stay in the loop on clinical decisions; and every decision has an audit trail. Controls map to HIPAA, HITECH, SOC 2, ISO 27001, and HITRUST.

How do you stop a clinical AI from hallucinating?

The language model never makes the clinical call. Deterministic rules and a knowledge graph decide; a safety agent checks contraindications; the LLM only writes the readable summary. Generation is grounded on your data, not the open web.

How fast can we see something real?

A governed proof of concept typically runs in weeks, not quarters – because the data foundation and compliance scaffolding come from production-tested components, not a from-scratch build.

What does the assessment commit us to?

Nothing. It’s a free 30-minute read of what data is usable today, what’s blocked and why, and which use cases could ship first – shared evidence for your clinical, data, and compliance leaders.