Recruit Faster. Deviate Less. Complete Trials on Schedule.
Zabrizon's AI platform accelerates patient recruitment, predicts site performance, monitors protocol adherence in real time, and automates regulatory documentation — reducing average trial timelines by 30% and protocol deviations by 45%.
Clinical Trial AI Capabilities
Intelligent automation across every phase of trial design, execution, and closeout.
AI-Powered Patient Recruitment & Matching
Machine learning matches eligible patients from EHR, claims, and registry data — dramatically cutting the time from protocol activation to enrolment.
- Protocol-to-patient matching across EHR and real-world data
- Pre-screening eligibility scoring with inclusion/exclusion criteria
- Site feasibility scoring by disease prevalence and investigator experience
- Patient portal recruitment and eConsent workflows
Real-Time Protocol Adherence Monitoring
Continuous monitoring of site data against protocol requirements — surfacing deviations before they become findings and flagging sites at risk of falling behind.
- Automated protocol deviation detection across all study data
- Visit window and procedure compliance tracking
- Site performance dashboards with risk stratification
- Automated query generation and resolution tracking
Regulatory Documentation Automation
AI-assisted generation of CSRs, study reports, and submission-ready documents — reducing regulatory writing burden and accelerating IND, NDA, and BLA timelines.
- Auto-population of CRF data into report templates
- ICH E6 GCP compliance checking and audit trail
- eTMF document management and completeness scoring
- Automated CIOMS/MedDRA coding for adverse event reporting
Decentralised Trial (DCT) Support
Infrastructure for hybrid and fully decentralised trials — remote consent, wearable data ingestion, telemedicine visit integration, and home nursing coordination.
- eConsent and remote patient onboarding
- Wearable and IoMT data collection and EDC integration
- Telemedicine visit scheduling and protocol capture
- Home health coordination and specimen logistics
AI Support Across the Full Trial Lifecycle
From protocol design to regulatory submission — Zabrizon's AI is embedded at every stage.
Protocol Design
AI-assisted eligibility criteria optimisation and feasibility modelling
Site Selection
Predictive site performance scoring and feasibility assessment
Patient Recruitment
EHR/RWD matching, eConsent, and pre-screening automation
Data Collection
EDC integration, protocol monitoring, and query automation
Regulatory Submission
CSR generation, eTMF management, and submission automation
Regulatory & GCP Compliance
Built to meet global regulatory requirements for clinical data integrity and trial operations.
Ready to Run Faster, Smarter Clinical Trials?
See how Zabrizon's AI reduces your trial timelines and protocol deviation rates from day one.
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