Held-out validation
We build to medical-device standards because that’s what patients deserve.

Gosta Studio helps clinical teams tailor documentation to their needs, while Gosta Insights gives authorized leaders a real-time view of adoption, activity and note quality.
The factory is a cycle, not a line. Surveillance findings from live clinical use become retraining data and new success criteria for the next training round on LUMI.
Every model is measured against the clinical success criteria it was commissioned for — before it ever reaches a patient record.
We build to medical-device standards because that’s what patients deserve.
Critical health infrastructure should not depend on non-European providers.
For every model, we define where it must not be used. Knowing a model’s limits is part of the model.
Limited pilots with named clinical owners, defined metrics, and a rollback plan — deployment is a change in clinical workflow, not a software release.
European healthcare regulation isn’t an obstacle to route around — it’s the specification we build to. Owning the full stack is what makes certification possible.
The sovereign model pathway enables development and certification of clinical AI as a medical device under the Medical Device Regulation.
A full AI Management System governs the lifecycle of every model — high-risk AI obligations engineered into the platform, not bolted on.
EU-hosted training on LUMI, local inference inside hospital environments. Patient data stays where it belongs.
The Gosta Research Program offers academic and non-commercial researchers free access to our clinical AI models — OCR, de-identification, clinical coding, structured extraction — across five languages. Hosted by us, or deployed in your own GPU infrastructure.

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