What the platform does today.
Everything below is available to a user right now. It’s checked against the running code rather than maintained by hand, so if a capability disappears the check fails before this page can go on claiming it.
Last reconciled with the code on 25 August 2026.
Available now.
01
CTCAE grading, v5 and v6
Every adverse event in a note is graded against the CTCAE version the protocol names, with both versions live on one engine.
02
Causality attribution per drug
Each event is scored for attribution against every drug in the regimen, using WHO-UMC and Kramer, with the reasoning shown.
03
Citation on every grade
Each grade traces to the line in the medical record that produced it, and a grade whose citation set is incomplete is flagged before it is signed.
04
Regulatory report generation
The platform produces FDA MedWatch, IRB and serious adverse event reports from the graded record, and they download as documents.
05
21 CFR Part 11 electronic signature
A grade becomes a record when a qualified investigator signs it, and the signature carries what was accepted, what was overridden and the citation set as signed.
06
Medical record integration, both directions
Notes are imported from the medical record, and graded output is written back to it.
07
Blind grading, adjudication and agreement
Multiple raters grade the same case without seeing each other, disagreements route to an adjudicator, and inter-rater agreement is measured.
08
Calibration training for coordinators
A coordinator grades a synthetic case and compares against the engine criterion by criterion, with an educator composing the case set and tracking competency.
09
Sponsor safety surface
A sponsor reads graded safety data for their own trials, separately from the site view.
10
Patient capture between visits
A patient records what happened between visits in their own words, in seven languages, by voice or text, and it is carried into the next clinical encounter.
11
Pre-visit interview
The questions a coordinator would ask are gathered before the visit and presented for verification and sign-off.
12
Patient-reported outcome instruments
A sponsor composes an instrument battery for a study, schedules it, and publishes it to participants without an application release.
13
Protocol ingestion
A protocol document is read into structured form, so grading runs against what the protocol actually names.
14
Export and audit trail
The graded record exports for a sponsor or a monitor, and every access to patient data is recorded.
15
Ambient recording in the room
A visit is recorded and turned into a note, so the clinician is not typing while the patient is talking.
Not yet, and we won't say otherwise.
These are specified or partly built. They aren’t available to you, so you won’t find them claimed anywhere else on this site either.
Quality of life scoring
Standard quality of life instruments, scored and trended alongside the graded record. The instrument layer is built and the scoring engine is specified; this is not yet something a reader can use, which is why it is not claimed in the headline.
Pre-visit interview by telephone
The pre-visit questions asked over the phone rather than in a room. Sequenced behind the ambient scribe, and gated on asking patients whether they want it.
Subject registration written outward to the study database
Register a trial subject once here, and have it written to whichever electronic data capture system the site runs.