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.
Less monitoring time
0 %
Faster query close
0 x
PII exposed
0
To database lock
0 days

ProCTTH is changing the future of the clinical trial ecosystem by integrating end-to-end clinical trial flow through technology — with, clinical sites at the center.

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."

P. Andersson
VP Clinical Operations · Mid-size CRO

Faster studies. Cleaner data.