DOCUMENT · CLINICAL TRIAL OPERATIONS

AI Scribe
for clinical trials.

Turn clinical conversations into structured documentation, with participant consent and clinician review at the centre.

Explore your trial’s needs

Be in the moment. Keep every detail.

DOCUMENT · CODE · COMPLY

Ambient documentation for investigators, research nurses, coordinators, phlebotomists, and home teams.

What it does in a trial 4 capabilities
  • Capture contemporaneous, consistent, attributable documentation
  • Capture information once for both the source record and trial database
  • Prepare structured, EDC-ready data and coding suggestions for review
  • Require review and approval by an authorised professional before any document enters the record
Why it matters
  • Support every professional who touches a participant
  • Keep clinical attention on the encounter
  • Create a consistent documentation structure across roles and settings
  • Keep professional judgement and approval at the centre

Documentation for every role.

Everyone who touches a participant. One consistent record.

PIs & SUB-Is

Investigators

  • Visit source notes
  • Adverse event narratives and causality notes
  • Protocol deviation notes
  • GP and referral letters
CLINICAL STAFF

Research nurses

  • Assessment documentation
  • Dosing and administration notes
  • Safety observation records
  • Participant education notes
SITE OPERATIONS

Coordinators

  • Visit reports and checklists
  • Contact and follow-up logs
  • Structured, EDC-ready data
  • Coding suggestions for review
MOBILE & DECENTRALISED

Phlebotomy & home teams

  • Sample collection documentation
  • Home-visit encounter notes
  • Chain-of-custody detail capture
  • Hands-free documentation on the move

Every document is reviewed and approved by an authorised professional before it enters the record. Contemporaneous, consistent, attributable documentation, captured once for the source record and trial database.

Captured once. Structured for the source record and trial database. Reviewed and approved by an authorised professional.

Less time documenting. More attention for the person. Each module works within Nurial’s shared operational intelligence layer, connecting participant engagement, visit preparation, documentation and trial oversight.

08 / WHAT COMES NEXT

Your next trial.
A new
possibility.

Let’s map Nurial to your next protocol. A working session with your operations team is enough to model the impact — site by site, visit by visit, against your own protocol and budget.

info@nurial.co.uk
A conversation about your trial. A plan built around it.
LET’S BUILD SOMETHING BETTER

Start a conversation.

Tell us a little about what you’re working on.

Your enquiry goes directly to our team at info@nurial.co.uk. We’ll use your details to reply to your message.