Castor Catalyst: Generate Regulatory-Grade, Real-World Evidence With Unprecedented Speed And Efficiency Using Castor's AI-Automated Extraction Model.

Manual data abstraction and source data verification remain major cost drivers in clinical trials, often consuming more than half of a Phase IV study budget and delaying timelines by months. A modern, AI-driven approach transforms this process by automating data extraction directly from EHR and claims systems, ensuring regulatory-grade accuracy while eliminating transcription errors. With patient consent and secure retrieval protocols, structured CDISC-compliant outputs are generated rapidly, supported by a visual audit trail for full traceability.

This model delivers measurable impact — up to 80% cost reduction and study completion 70% faster than traditional methods. For teams managing real-world evidence or post-market studies, automation offers a scalable solution to streamline workflows, maintain compliance, and accelerate decision-making. Download the full resource to see how automation redefines evidence generation and reduces trial complexity.