Maintain detailed profiles of all your clinical trial sites. Store site contact information, principal investigator details, and site-specific notes with quick access to site history and performance metrics.
Comprehensive visit scheduling with calendar integration. Step-by-step visit workflows customized to your protocols. Digital checklists ensure protocol compliance and consistent monitoring.
Precise time tracking for all monitoring activities. Digital time cards with automatic calculations. Category-based task organization for accurate reporting that meets regulatory requirements.
Track and categorize all study-related expenses. Streamline reimbursement processes with organized documentation and easy export capabilities.
Intuitive booking interface for scheduling site visits. Conflict detection to prevent scheduling errors. Automated reminders for upcoming visits and deadlines.
Customizable templates for different study protocols. Data visualization to identify trends and potential issues. Export capabilities for sharing with study teams and sponsors.
Protocol-specific calculators and reference guides. Regulatory document checklists and templates (ISF). GCP compliance helpers and study metrics indicators.
Direct messaging with study teams. Secure communication channels that maintain compliance. Keep all project communication organized in one place.
End-to-end encryption for all data. Regular security audits and updates. HIPAA, GDPR, and 21 CFR Part 11 compliance built-in.
Reduce administrative time by up to 40% with automated processes and streamlined workflows.
Digital checklists and reminders ensure nothing is missed during site visits and monitoring activities.
Standardized processes lead to more consistent monitoring and higher quality data collection.
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