Consolidating Prolog & Compliance to Slash Delays in Clinical Trials
We are a small, agile team on a mission to dramatically reduce the outrageously high rate of delays in clinical trials and the manufacturing of FDA-regulated products. By merging the power of Prolog-based formal methods with cutting-edge compliance technology, we’re transforming regulatory processes into a seamless, verifiable journey.
Our Vision
We envision a world where regulatory compliance isn’t a bottleneck, but a catalyst for innovation. Our mission is to eradicate delays that hinder clinical progress and product approvals—ensuring life-saving therapies reach patients faster.
Our Approach
By leveraging formal methods and Prolog-based reasoning, we consolidate complex regulatory requirements into precise, verifiable models. Our rapid, iterative process enables continuous improvement—transforming compliance into an automated, reliable component of your workflow.