01
Author documents
From protocols to patient information sheets, SOPs, and investigator brochures, Cori helps you produce first drafts of trial documents in minutes instead of weeks.
Powered by our best-in-class authoring tool, you can adapt each draft to your study needs, apply your own templates, and refine content as you go, keeping you in full control of the process.
03
Review faster
Cori reviews documents for regulatory compliance, GxP, quality, and patient-focused requirements, helping you de-risk trials from the start.
It works alongside your team, flagging issues and inconsistencies early, suggesting improvements, and reducing costly amendments. So you move to submission with fewer and shorter review cycles.
Accelerate trial timelines, reduce regulatory risk, and scale your studies with confidence. Optimize your operations, streamline client collaboration, deliver trials faster, and ultimately unlock higher profitability.
Simplify trial documentation, quickly set up compliant studies, and spend more time on your science. Accelerate your path to market, expand your resources, and take control of your trials.
"For emerging life science companies, navigating trial documentation can be overwhelming. Cori provides the structure and intelligence needed to speed up while maintaining compliance."
An van Es-Johansson
Former CMO & Clinical Development Leader
