Streamlined Clinical Data Collection
Our eCRF platform simplifies the process of collecting, managing, and analyzing clinical research data.
Main Portal
Access study selection, dashboards, subject matrices, and eCRF forms.
Admin Portal
Manage studies, users, and system configuration.
Platform Features
Our comprehensive eCRF platform offers everything you need for efficient clinical data management.
Study Management
Create, configure, and manage multiple clinical studies with flexible protocol definitions.
Subject Matrix
Comprehensive matrix to monitor enrollment, visit completion, SDV status, and sign-off.
eCRF Forms
Intuitive per-visit electronic case report forms with a streamlined data entry wizard.
Adverse Events
Track and manage adverse events and serious adverse events with full lifecycle workflows.
Concomitant Medications
Record concomitant medications with versioned amendment tracking and AE relationship linking.
SUSAR Management
Generate and manage SUSAR cases with CIOMS formatting and regulatory reporting.
Data Quality
Configurable rule engine with real-time alerts, severity scoring, and lifecycle management.
Real-Time Dashboards
Interactive dashboards providing real-time insights into study progress and subject statistics.
Data Export
Comprehensive export with audit history, source data verification, and decoder integration.
Sovereign Platform
Deploy on your infrastructure to meet data residency and regulatory compliance requirements.
RBQM
Risk-based quality management with centralized oversight and data-driven monitoring signals.
International Standards & Submission Readiness
CDISC-compliant data models with submission-ready exports for regulatory authorities worldwide.