Clinical research operations workspace
Welcome to CRA AI Assistant
Your AI-powered companion for clinical trial monitoring worldwide.
Workspace ready
Reports, regulations, CRA tools, and learning resources are available.
19
CRA Tools
101
Regulations
14
Languages
30
Learning videos
Use as a clinical operations assistant
CRA AI Assistant helps organize reports, reference regulations, and support monitoring workflows. Always verify outputs against the protocol, source records, SOPs, and official FDA/ICH documents before use.
Features at a Glance
A clean overview of the core workflows available in the assistant.
Site Visit Report Generator
Convert field notes into professional ICH GCP-compliant site visit reports with AI-powered formatting and regulatory citations.
FDA/ICH Q&A (RAG)
Ask questions about FDA regulations, ICH GCP guidelines, and clinical trial compliance. Get cited answers from 100+ indexed documents.
CRA Toolkit (19 Tools)
Visit scheduler, deviation log, SDV tracker, TMF documents, enrollment dashboard, site scorecard, contact list, and more.
Learning Center
Watch video tutorials from Clarity Clinical Solutions. Track your learning progress. Perfect for on-the-go study.
Contact & Consulting
Connect with Clarity Clinical Solutions LLC for professional clinical research consulting services.
Quick Start Guide
Start with the task you need now, then move between tools as your monitoring work evolves.
1Generate a report from Tab 1 by entering field notes and clicking Generate Report.
2Ask regulatory questions from Tab 2 and review cited answers.
3Use the CRA tools from Tab 3 to manage visits, sites, and tracking tasks.
4Open Tab 4 to watch tutorials or track learning progress.
5Use Tab 5 when you need consulting support or more information.
❓ Frequently Asked Questions
Common questions about CRA AI Assistant