Clinical documentation and ambient scribing
Assistants that draft notes from a consultation so clinicians spend time with patients, not paperwork. The clinician reviews and signs every note, keeping a human firmly in control of the record.
AI for providers, payers and health-tech. From clinical documentation to patient navigation and operational efficiency, we build compliant, auditable AI for European healthcare.
Healthcare generates vast clinical and operational data, faces acute staffing pressure, and works under strict privacy and safety regulation. That combination makes it one of the highest-value and most carefully governed settings for AI.
European providers must satisfy GDPR, medical-device rules and the EU AI Act, where many clinical uses are high-risk. The value comes from AI that reduces administrative load and supports clinicians, without ever replacing clinical judgement.
From the clinic to the back office, these are the use cases that free clinician time and cut administrative cost, safely.
Assistants that draft notes from a consultation so clinicians spend time with patients, not paperwork. The clinician reviews and signs every note, keeping a human firmly in control of the record.
Information-only assistants that help patients find the right service and answer common questions, escalating anything clinical to a person.
Extraction and coding from referrals, letters and forms, routed into your systems with a human check on the uncertain cases.
Demand, capacity and no-show forecasting that helps you plan staffing and reduce waiting times.
Audit trails, explainability and bias monitoring so clinical AI meets EU AI Act and medical-device expectations.
EU AI Act complianceHealthcare AI has to be safe, private and explainable before it is anything else. We build with data protection and clinical governance at the core, keep a clinician in the loop for anything that touches care, and design for on-premises or private-cloud deployment where the data demands it.
Every engagement starts with the data, the risk classification and the clinical workflow. We build for GDPR and EU AI Act conformity by design and deliver systems that hold up to clinical and regulatory scrutiny.
Often yes. Many clinical uses are treated as high-risk, and some overlap with medical-device regulation, so they need risk management, audit trails and human oversight. We build for that from the start.
No. We build AI that supports clinicians by removing administrative load and surfacing information. A clinician reviews and signs off anything that affects care.
With data minimisation, encryption and, for sensitive workloads, on-premises or private-cloud deployment with European data residency, so patient data stays under your control.
A production system is typically eight to sixteen weeks, delivered in phases so value arrives early and each step can be validated clinically.
You do, under EU contract law, with GDPR and EU AI Act obligations handled under one legal regime.
A 30-minute call. We map your highest-leverage, lowest-risk AI use case in healthcare and outline a pilot you can validate clinically.