MediScribe AI
A clinician and patient in a quiet consultation room

MediScribe AI

Clinical notes for the most sensitive conversations.

Clinician-reviewed documentation for sexual and reproductive health. Nothing enters the record until you approve it.

Designed for sexual health workflows

Generalist scribes optimise for broad care. Sexual health is different.

An illustrative clinician working on a laptop

Informed capture

The patient is told and can decline. Recording stops when you stop it.

Structured SRH drafts

Notes mapped to your proforma, GUMCAD and SRHAD fields.

Clinician-reviewed notes

Every line linked to its source. Nothing exported until you confirm.

Built around your record

We start with your fields, not a generalist summary.

How MediScribe AI works

The minimum trustworthy workflow. Three steps. The clinician owns the third.

  1. 01

    Informed capture

    The patient is told and can decline. You control what is recorded.

  2. 02

    Structured draft

    A proposed note mapped to your proforma and reporting fields.

  3. 03

    Clinician approval

    Every line linked to its source. Nothing exported until you confirm.

Data & security

Governance is product work.

Safety, data protection and evidence, built with the software.

See how we approach safety and governance
  1. 01

    Privacy by design

    A DPIA template built alongside the software, so your review never starts from a blank page.

  2. 02

    Clinical safety

    A DCB0129 safety case developed with the product.

  3. 03

    Evidence for your review

    DTAC evidence and an intended-purpose statement for your governance team.

  4. 04

    The clinician stays in control

    Documentation for clinician review. No clinical recommendations.

What the sector is saying

The guidance

NHS England guidance is in place, and the MHRA confirmed in July 2026 that documentation-only tools with clinician review are not medical devices.

Source

The evidence

An NHS England-sponsored evaluation of 17,000+ encounters found 23.5% more direct patient time.

Source

The scrutiny

Regulators and patients are finding errors in AI-written records. Clinician review is the product.

Source

Design partners

Two to four services. One pre-agreed evaluation.

A purchase path, not a free trial. No licence fee during evaluation, an independent evaluation and every governance artefact supplied. We ask for a clinical lead, eight to twelve clinicians and an honest decision at the end.

Register interest

If reviewing a draft takes as long as writing the note, we have not solved the problem. That is our test.

For patients: how MediScribe AI treats your information
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