From trial design to approved therapy
AI-powered trial design, predictive enrollment, regulatory automation, and a clinical data marketplace — unified in one platform.
10x
Faster protocol design
60+
Day enrollment lookahead
$68B
Addressable market
24/7
Autonomous monitoring
The Problem
$2.6B and 12 years to bring one drug to market
Disconnected tools, manual workflows, and data that never gets reused.
80%
of trials face enrollment delays
37%
of sites miss enrollment targets
$40B+
in trial data goes unused annually
Capabilities
One platform for the entire trial lifecycle
AI Trial Design
Adaptive, non-inferiority, and equivalence trials with Bayesian optimization.
Enrollment Intelligence
ML-powered site scoring, predictive modeling, and dropout risk analysis.
Regulatory Copilot
Automated IND/NDA/BLA gap analysis across FDA, EMA, and ICH.
Adaptive Analytics
Biomarker-guided interim analyses with real-time decision support.
Data Marketplace
Tokenized datasets with provenance, fractional licensing, and institutional access.
Autonomous Agents
AI agents that monitor trial health and optimize operations 24/7.
CTOS
Every capability, working together
Not a collection of tools — an integrated intelligence layer connecting design, execution, compliance, and monetization.
Learn about CTOS
Built for Healthcare
Purpose-built for clinical research
Every engine built from zero. Vertically integrated — no third-party API assemblies.
8 filings
Patent-pending IP
FDA / EMA / ICH
Regulatory coverage
3 continents
Engineering team
First T2T
Data exchange
Ready to see it?
Personalized demos for sponsors, CROs, and research sites.