Built for research site networks and health-system research institutes. Upload your de-identified trial files and wrldOS returns a monitoring- and inspection-readiness report — site risk pre-scored, deviations and essential-doc gaps surfaced before the monitor finds them. Protect your standing with sponsors and spare your team the visit scramble.
Delivered within 24 hours of upload · Human-reviewed before release · First report $2,500, additional from $1,500
Health-system research institutes, multi-site networks, academic medical centers — you're the one being monitored and inspected.
CRAs, CTMs and clinical-ops staff prepping interim monitoring visits.
You upload de-identified files. As a safeguard, wrldOS re-checks for residual structured HIPAA Safe Harbor identifiers before analysis — a second net on top of your own de-identification.
Priced against monitoring economics, not generic SaaS. An unprepared visit costs a site twice: coordinator days lost to the scramble, and findings on the monitor's report that erode sponsor confidence in your site. The prep burden is documented — more than 80% of sites report spending 21+ hours on source-document preparation for high-complexity studies (Tufts CSDD · Applied Clinical Trials, 2026). One report pre-scores your risk and surfaces deviations and essential-doc gaps before the monitor arrives. And because source-data verification consumes ~46% of a CRA's on-site time (Applied Clinical Trials), a prepared site means a shorter, cleaner visit — and a sponsor more likely to bring you the next study.
Annual single-trial and multi-trial licensing for sponsors and CROs — multiple sites, multiple reports per year — talk to us. Additional reports from $1,500.
Send us one study. We'll prepare the AI Visit Prep Report and you'll see exactly what a monitor would flag — before they arrive.