CRA Ai Assistant
Clinical Monitoring Platform for CRAs

Less Admin. More Time for Monitoring.

Your all-in-one AI-powered workspace for clinical trial monitoring. Plan visits, track findings, manage essential documents, and prepare monitoring reports — all in one place.

Free 3-day trial included with your account.

Monitoring DashboardStudy #CR-2049

12

Active Sites

28

Visits

5

Open Findings

Site 004 — SIV VisitScheduled
Site 002 — Findings Follow-upResolved
Monitoring progress72%

Sound Familiar?

Common challenges CRAs face when monitoring workflows live across disconnected tools.

Too many spreadsheets

Managing study info, visit schedules and outstanding actions across multiple files.

Time-consuming report writing

Hours organising notes and preparing monitoring visit reports.

Difficult follow-up tracking

Keeping track of outstanding findings, site responses and action due dates.

Scattered documentation

Searching across folders and systems for essential documents and previous visit records.

CRA AI Assistant brings your monitoring workflow together.

Everything you need to monitor a trial

A focused toolkit built around the real CRA workflow — from planning to follow-up.

Visit Planning

Schedule PSV, SIV, IMV and COV visits and keep your preparation notes organised.

AI Report Assistant

Transform monitoring notes into structured report drafts the CRA reviews and edits.

Action Tracker

Monitor outstanding findings, assign responsibilities and follow up due dates.

Study & Site Management

Investigator details, site status and monitoring history in one place.

Document Management

Organise regulatory documents, training records and monitoring reports.

Monitoring Analytics

Monitoring progress, outstanding issues and site activity via clear dashboards.

See How It Works

Four steps from visit planning to closed actions.

1PLAN

Create a monitoring visit

Set up a PSV, SIV, IMV or COV visit and prepare your monitoring checklist.

2MONITOR

Record findings

Log findings and track review progress on site.

3GENERATE

Create a report draft with AI

Turn your monitoring notes into a structured report draft ready for your review.

4FOLLOW UP

Assign & track actions

Assign responsibilities, set due dates and monitor outstanding items to closure.

Who Is It For?

Built for the people who keep clinical trials running on site.

Independent CRAs

A single workspace to organise studies, sites and visits without spreadsheets.

Full-time Clinical Research Associates

Plan visits, draft reports faster and keep on top of every outstanding finding.

Clinical Trial Managers

Visibility into monitoring progress, open issues and site activity across studies.

Small CRO Teams

Coordinate monitors with shared study data and consistent reporting workflows.

Simple, transparent pricing

Choose the plan that fits your monitoring workload. Cancel anytime.

Starter

For independent CRAs managing a few studies

$29/month
  • Up to 5 active studies
  • Site & visit tracking
  • Findings & CAPA management
  • Document scanning
  • Email support
Most popular
Professional

For full-time CRAs and small monitoring teams

$79/month
  • Unlimited studies & sites
  • AI Monitoring Assistant
  • Pill counting tool
  • Google Calendar integration
  • Email support
Enterprise

For CROs and large monitoring organizations

Custom pricing

Starting from $499/month

  • Everything in Professional
  • Up to 10 concurrent monitors in the base package
  • Additional monitor seats available
  • Larger teams can negotiate higher limits
  • Advanced analytics & reporting
  • Dedicated account manager
  • Priority support
  • Custom onboarding
  • Flexible annual contracts
Contact Sales

Beta tester? Enter your code before subscribing to Professional.

Starter and Professional are billed monthly or annually (annual saves about 17%). Enterprise uses custom pricing — contact sales for a quote. You can cancel any subscription at any time — access continues until the end of your current billing period. New accounts include a 3-day free trial to explore the platform before subscribing.

Trust & Security

Designed to support structured clinical monitoring workflows, with human review and oversight at every step.

Data protection

Uploaded documents and files are stored in private, access-controlled storage — not public links.

User access controls

Each CRA sees their own studies, sites and findings. Access is tied to your authenticated account.

Human review of AI output

AI-generated report drafts are suggestions. You review and edit every word before anything is final.

You control your data

You create, edit and delete your reports, findings and monitoring records at any time.

CRA AI Assistant is a workflow tool. It does not replace the clinical judgement, regulatory responsibilities or oversight of the study team.

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Frequently Asked Questions

Ready to Simplify Your Monitoring Workflow?

Spend less time managing administrative tasks and more time focusing on your clinical research activities.