ProCTTH meets each stakeholder where they work. Sites get an engagement-first eSource; sponsors and CROs get a blinded eCRF with real-time operational visibility on the same unified data model.
Capture source data once, schedule visits, chat with subjects, and reward retention, all while subject identity stays at the site.
21 CFR Part 11, GCP, HIPAA, and GDPR on day one, with a validation pack ready to ship.
Subjects, visits, devices, and audit events live in a single schema. No per-study silos or exports.
E-consent, home visits, IoT capture, and mobile engagement ship out of the box.
Deploy to EU, US, India, Japan, or Canada with regional data residency controls.
Super Admin, Admin, Study Admin, Member, Investigator, CRA, CRC, and Subject. All scoped.
Protocol-to-form generation, eligibility matching, and drop-off prediction reviewer-in-the-loop.
