Every capability you need to run a hybrid or decentralized trial; built natively on a single data model, secured by design, and configurable in hours.
Configure protocols, visits, and forms without programming. Drag-and-drop with conditional logic and edit checks
Calendar-view schedule of assessments. Window math, dependencies, and amendments versioned automatically.
30+ field types, validations, derivations, repeating sections, and library forms reusable across studies.
Multi-language electronic informed consent with comprehension checks and signed PDF audit trail.
Streamline self-service enrollment with eligibility assessment and investigator approval workflows.
Visit reminders, missed-visit escalations, AE/SAE alerts, and emergency broadcasts to roles or cohorts.
Secure video calls between subjects and investigators, with dedicated chat between subjects and CRCs, and between investigators, CRCs, and CRAs.
Subjects choose at-home or on-site visits. Sites and labs receive readiness notifications.
Smartwatches and connected devices help capture subject vitals for clinical study monitoring.
Monitor subject engagement, adherence, and potential drop-off risks, enabling site staff to take timely action.
Milestone-based subject compensation that drives retention without manual reconciliation.
Sponsors and CRAs see clean data with subject identity protected at the source.
ProCTTH is a single platform, not a stitched-together suite. That means one identity, one audit trail, one upgrade path.
Subjects, visits, forms, devices, and audit events live in one schema; no per-study silos
Stream-first ingestion. Data captured at the bedside is queryable in under a second.
Eligibility matching, AE Reporting, and form generation run directly within the platform.
Form revisions, edit checks, and consent versions are all branch-able.
ProCTTH organizes everything around users and their roles; granular, auditable, and aligned with how research teams actually work.
Org-level control
Site administration
Per-study setup
Operational access
A single pipeline moves data from capture to analysis.
Site enters source data once. IoT devices show vitals. Subjects submit ePRO in-app.
Edit checks, range validations, and cross-form rules fire as data lands.
CRAs review queries, flag deviations, and sign off remotely or on-site.
Database lock in days. Export study data for analysis.
Exports for decision making and analysis
Isolated instance for enterprise sponsors.
Active-active infrastructure.
TLS 1.3 in transit, field-level role based blinding for PII.
Yes, study designers can enable paper-to-source workflows for specific sites or regions when required by IRB/EC.
Data is frozen and export is generated for retention windows you configure.
Most studies activate in 2-3 weeks, including protocol configuration, form setup, and site training.
