Safety by design
A language model can sound sure about something wrong. Cognivolt is built on one principle: the AI writes, independent checks verify, and the clinician decides.
Four layers between the consultation and your signature
Writing the note
The note is written from the consultation, in your format, recording what was said.
Independent safety checks
Doses, measurements and scale scores are checked against what was actually said, and allergy and drug interaction checks use fixed reference tables (Standard). None of it is left to the AI.
The audit agent
A final AI review of the whole output against the consultation, before anything reaches you.
The clinician
You weigh the differential considerations, confirm the diagnosis and approve the note. Codes, guidelines, psychoeducation and rating scales wait for your diagnosis.
Patient data
Consent is confirmed before every recording, audio is permanently deleted once the note is written, and records are stored in the EU and encrypted at rest, with every access logged. See where patient data goes.
The limits, honestly
Any AI can make mistakes. These checks reduce errors; they do not remove the need for review. Reference tables flag the interactions they list, and the clinician remains responsible for the final note. That is why every note is a draft until you approve it.
In detail
Frequently asked questions
Is Cognivolt safe to use for clinical documentation?
Cognivolt is built so that every note is checked before you see it, prescribing checks are kept apart from the AI, nothing depending on a diagnosis is generated before you confirm it, and every note stays a draft until you approve it.
How does Cognivolt keep safety checks apart from the AI?
Doses, measurements and scale scores are checked against the consultation outside the AI, and allergy and interaction checks are lookups in fixed reference tables. A final AI audit layer then reviews the whole output before you see it.
What are the limits of Cognivolt’s checks?
They reduce errors; they do not remove the need for review. Reference tables flag the interactions they list, and the clinician stays responsible for the final note.
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