The right trial sites, the right patients, right now
Access exclusive clinically rich data
Leverage real-world data from the American Academy of Ophthalmology IRIS® Registry (Intelligent Research in Sight) and the American Urological Association (AUA) Quality (AQUA)® Registry. Utilize curated codelists and clinical assessments derived from structured and unstructured EHR data.
Intuitive protocol builder
Build cohorts with a user-friendly interface to efficiently model study protocols and identify optimal sites based on inclusion and exclusion criteria. No coding expertise necessary!
Reduce recruitment timelines
Pinpoint eligible patient populations and high-volume trial sites in minutes. Identify and connect with sites that have the right mix of research experience and patient availability to serve as a trial site or a potential referral source.
Advance diversity in clinical trials
Identify practices with patients in specific underrepresented racial or ethnic groups. Set informed enrollment targets for specific demographic subgroups.
Let’s Get Started!
Contact us today to learn how our data-driven approach can accelerate your clinical trial.