Automation Softwarefor Clinical Trials
Agentic workflows that validate every trial document against your protocol.
Founded by Physicians.
Powered by AI.
Built by the team who ran the trials. MDs and PhDs from Recursion, GSK, AstraZeneca, Genentech, University of Cambridge, and University of Oxford. We have designed trials, managed CROs, and sat through protocol amendment chaos. Now we are building the infrastructure we wish existed.
Accelerating Clinical
Trial Startup
Trial startup is the longest and most expensive bottleneck in clinical operations.
Compress startup time from 8 months to 8 weeks.
Executive Leadership
- Accelerate time to first patient and preserve runway.
- Reduce startup consulting fees up to 80%.
- Improve control of scope and timelines.
Clinical Operations
- Convert protocol content into structured operational work.
- Standardize vendor requirements.
- Focus on strategic decision-making.
Finance Management
- Transparent budgeting.
- Visibility into cost drivers and timeline risks.
- Stronger and auditable startup inputs.
How Our Platform Works
Analyze protocols. Validate every vendor agreement, document and amendment against them. Compress 8 months to weeks.
What Makes Us Unique
End-to-End Platform
Complete trial startup in one place. Not scattered across spreadsheets and emails.
You Stay in Control
System flags issues, you make decisions.
Audit-Ready by Default
Complete audit trail with protocol traceability for regulatory inspection.
