A blinded eCRF with real-time visibility.
Get clean, audit-ready data without ever exposing subject identity. One platform for protocol design, site management, monitoring, and reporting — across hybrid and decentralized trials.
From protocol to database lock.
Real-time eCRF
Clean data flows from site to sponsor the moment it's captured. No batch uploads, no SDV bottleneck.
Blinded by design
Subject identity is protected at the source. CROs, CRAs, and sponsors never see PII — only study data.
21 CFR Part 11 + GCP
Audit trail, e-signatures, role-based access, and HIPAA-compliant infrastructure out of the box.
Configurable edit checks
Build query workflows, range checks, and cross-form validations without programming.
Decentralized-ready
e-Consent, e-enrollment, home visits, and IoT device capture make hybrid and DCT designs effortless.
CRA mobile monitoring
Remote and on-site monitoring from a single app. Encrypted chat & video with investigators.
The cockpit for your portfolio.
KRI dashboards
Pre-built risk indicators on enrollment, queries, AE rates, and protocol deviations.
Cross-study libraries
Reuse forms, edit checks, and visit templates across your portfolio.
Multi-region deploy
Pin studies to EU, US, India, Japan, or Canada for residency compliance.
Database lock fast-track
Real-time SDV means lock in days, not weeks.
"We replaced an EDC, an eConsent vendor, and an ePRO platform with one ProCTTH instance. Operations and IT thanked us in the same week."
Faster studies. Cleaner data.
- Cross-study libraries and form templates
- AI-assisted protocol design
- One platform — no integrations to maintain
- Global deployment with regional data residency
- Validation pack & SOC 2 reports on demand
- Open API for downstream BI and SAS pipelines