Eight engines. One platform.

AI trial design

Smarter trials from day one — protocols that adapt as the data arrives.

• Non-inferiority / superiority / equivalence engines
• Adaptive design optimization
• Sample size calculator with power analysis
• Protocol deviation predictor

Patient recruitment intelligence

Predict enrollment bottlenecks before they happen.

• Site performance scoring and benchmarking
• Predictive enrollment modeling
• Dropout risk analysis and early warning
• Diversity and inclusion tracking

Regulatory copilot

Automate the most labor-intensive parts of submission preparation.

• Automated IND/NDA/BLA gap analysis
• FDA / EMA / ICH submission assistant
• Compliance matrix tracking
• Amendment impact assessor

Universal report generator

Publication-grade reports with adaptive statistical methods.

• Automated interim and final clinical study reports
• Adaptive signal detection
• Real-time DSMB dashboards

Clinical data marketplace

Unlock the value of clinical data through secure, compliant licensing.

• Sponsor-to-buyer data licensing
• De-identified dataset packaging
• Provenance and audit trail
• Institutional access tiers

Trial-to-token framework

The first tokenized clinical data exchange — provenance and liquidity for trial data.

• Tokenized clinical data assets
• Fractional ownership and licensing
• On-chain provenance tracking
• Marketplace liquidity layer

Agentic orchestration

Autonomous AI agents that monitor, optimize, and execute operations 24/7.

• Multi-agent workflow engine
• Autonomous trial monitoring agents
• Alert escalation and DSMB notification
• Integration with external EHR/EDC systems

Adaptive intelligence engine

Real-time biomarker analysis that triggers protocol adaptations.

• Real-time biomarker-guided adaptation
• Interim analysis triggers
• Endpoint reassessment module