MediScribe AI

The workflow

Capture only what is permitted. Structure the draft. Keep the clinician in control.

Three steps. The clinician owns the third.

A clinician reviewing a structured draft note on a laptop
  1. 1

    Informed capture

    The patient is told first and can decline at no cost to their care. Capture controls stay on screen; the clinician can pause, stop or exclude a section at any time. Audio is not kept beyond transcription unless your DPIA says otherwise.

  2. 2

    Structured draft

    A speech model tuned for UK accents and sexual health vocabulary transcribes the consultation. Concepts are linked to SNOMED CT and the draft is laid out in your proforma, including GUMCAD and SRHAD items. Gaps are flagged, never guessed.

  3. 3

    Clinician approval

    Every line links to its source in the transcript. Missing fields and uncertain statements are highlighted. The clinician edits and confirms; nothing is exported until then, and nothing saves in the background.

Into the record

Approved notes reach your sexual health EPR as structured fields, not pasted text. We are testing Lilie and Inform integration with design partners; until then, a structured copy route avoids re-typing.

What MediScribe AI does not do

No clinical recommendations, diagnostic outputs, risk scores or chatbot. Safeguarding decisions stay with the clinician. The intended purpose is documentation for clinician review, which keeps it outside medical device classification under the MHRA’s July 2026 guidance.

Who it is for

Doctors, specialist nurses, health advisers and healthcare assistants in integrated sexual health services. Face-to-face first; telephone and video to follow.

How it arrives in a service

Governance pack and DPIA in the first fortnight, clinical safety review and EPR set-up by week three, a 30-minute training session, a shadow week, then go-live with weekly usage reports.

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