Process Automation for Clinical Research Organizations (CROs)
True process automation in clinical trials begins with solving the biggest bottleneck: manual document collection. Stop chasing endless paperwork and start accelerating your research timelines.
Request a Demo →Why Leading CROs Automate Their Document Collection
Our platform is engineered to tackle the unique document challenges of clinical research, from site initiation to trial close-out, ensuring both compliance and speed.
AI-Powered Compliance & Validation
Our AI automatically analyzes critical documents to validate them for completeness, authenticity, and expiration. Ensure regulatory compliance and audit-readiness from day one.
Automated Site & Patient Reminders
Eliminate the manual work of chasing documents. Our system automatically sends reminders to end-clients, notifying them of outstanding or invalid documents to keep your trial on schedule.
Centralized Status Tracking
Gain complete visibility with a real-time dashboard. Track the status of every document from every end-client, identify bottlenecks, and get instant notifications on status changes.