Features
Multi-agent clinical trial design
Protocol outline generation
Patient enrollment forecasting
Endpoint selection rationale
Regulatory compliance checklists (FDA, EMA, ICH)
Literature search and evidence synthesis
Feasibility assessment reports
Export to Word, PDF, and CDISC SDTM format
Adaptive trial design templates (Bayesian dose-finding)
Rare disease agent workflows with natural history comparisons
Custom agent building via no-code editor
API access for enterprise integrations (Professional plan)
Version control and audit trail
Real-time collaboration for design teams
Therapeutic area-specific templates (oncology, neurology, rare diseases)
AI-powered patient identification from EMRs
Natural language processing on unstructured clinical notes
Real-time eligibility screening
Automated patient-trial matching
Integration with clinical trial management systems
Scalable cloud-based platform
HIPAA-compliant data handling
Customizable trial criteria input
Reporting and analytics on recruitment metrics
