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

MediScribe AI
Clinician-reviewed documentation for sexual and reproductive health. Nothing enters the record until you approve it.
Generalist scribes optimise for broad care. Sexual health is different.

The patient is told and can decline. Recording stops when you stop it.
Notes mapped to your proforma, GUMCAD and SRHAD fields.
Every line linked to its source. Nothing exported until you confirm.
We start with your fields, not a generalist summary.
The minimum trustworthy workflow. Three steps. The clinician owns the third.
The patient is told and can decline. You control what is recorded.
A proposed note mapped to your proforma and reporting fields.
Every line linked to its source. Nothing exported until you confirm.
Data & security
Safety, data protection and evidence, built with the software.
See how we approach safety and governanceA DPIA template built alongside the software, so your review never starts from a blank page.
A DCB0129 safety case developed with the product.
DTAC evidence and an intended-purpose statement for your governance team.
Documentation for clinician review. No clinical recommendations.
NHS England guidance is in place, and the MHRA confirmed in July 2026 that documentation-only tools with clinician review are not medical devices.
SourceAn NHS England-sponsored evaluation of 17,000+ encounters found 23.5% more direct patient time.
SourceRegulators and patients are finding errors in AI-written records. Clinician review is the product.
SourceDesign partners
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 interestIf 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