Twelve modules. One platform.

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.

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.

Pick what you need. Use it together.

No-Code Study Builder

Configure protocols, visits, and forms without programming. Drag-and-drop with conditional logic and edit checks

Schedule of Visits

Calendar-view schedule of assessments. Window math, dependencies, and amendments versioned automatically.

Visit Form Builder

30+ field types, validations, derivations, repeating sections, and library forms reusable across studies.

e-Consent

Multi-language electronic informed consent with comprehension checks and signed PDF audit trail.

e-Enrollment

Self-service enrollment with AI eligibility matching and investigator approval workflows.

Notifications & Alerts

Visit reminders, missed-visit escalations, AE/SAE alerts, and emergency broadcasts to roles or cohorts.

Web Call & Chat

Encrypted video and chat between subjects, investigators, and CRAs — fully audited.

Lab Visit Scheduler

Subjects choose at-home or on-site visits. Sites and labs receive readiness notifications.

IoT & Wearables

Connect smart watches and medical devices to push vitals into visit forms in real time.

Behavior Monitoring

ML signals on engagement, adherence, and risk of drop-off — actioned by site staff.

ProCoins Compensation

Milestone-based subject compensation that drives retention without manual reconciliation.

Blinded eCRF

Sponsors and CRAs see clean data with subject identity protected at the source.

Built for scale, speed, and audit.

ProCTTH is a single platform — not a stitched-together suite. That means one identity, one audit trail, one upgrade path.

Unified data model

Subjects, visits, forms, devices, and audit events live in one schema — no per-study silos

Real-time pipeline

Stream-first ingestion. Data captured at the bedside is queryable in under a second.

Edge-first AI

Eligibility matching, anomaly detection, and form auto-generation run inside the platform.

Versioned everything

Protocol amendments, form revisions, edit checks, and consent versions are all branch-able.

Built on profiles, not silos.

ProCTTH organizes everything around users and their roles — granular, auditable, and aligned with how research teams actually work.

Super Admin

Org-level control

Admin

Site administration

Study Admin

Per-study setup

Member

Operational access

SubjectInvestigatorCRACRC

Machine learning that earns its place.

We use AI where it measurably reduces operational burden — never as marketing decoration. ProCTTH organizes everything around users and their roles — granular, auditable, and aligned with how research teams actually work.
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From bedside to database lock.

A single pipeline moves data from capture to analysis. No batch exports, no nightly ETL, no brittle integrations between vendors.

Capture

Site enters source data once. IoT devices push vitals. Subjects submit ePRO in-app.

Validate

Edit checks, range validations, and cross-form rules fire as data lands.

Monitor

CRAs review queries, flag deviations, and sign off remotely or on-site.

Lock & export

Database lock in days. CDISC-ready exports for SAS, BI, or downstream pipelines.

Plays well with your existing stack.

Open APIs, webhooks, and pre-built connectors keep ProCTTH in sync with your CTMS, EHR, labs, safety systems, and analytics.

CTMS connectors

Veeva, Medidata, and custom CTMS sync for sites and sponsors.

Central labs

HL7 and FHIR feeds from LabCorp, Quest, and regional labs.

Wearables & IoT

Apple HealthKit, Fitbit, Withings, and Bluetooth medical devices.

Safety systems

AE/SAE push to Argus, ArisGlobal, or a custom safety endpoint.

BI & analytics

CDISC SDTM exports, S3 sync, Snowflake, and BigQuery destinations

SSO & identity

SAML 2.0, OIDC, Okta, Azure AD, and SCIM provisioning.

Audit-ready from day one.

Global, regional, or single-tenant.

BI & analytics

CDISC SDTM exports, S3 sync, Snowflake, and BigQuery destinations

Single-tenant option

Isolated instance for enterprise sponsors.

99.95% uptime SLA

Active-active infrastructure with automated failover.

Encryption everywhere

TLS 1.3 in transit, AES-256 at rest, field-level encryption for PII.

Common questions.

How fast can we go live?
Most studies activate in 2–4 weeks, including protocol configuration, form library reuse, and site training.
No. Identity lives at the site. Sponsors and CROs work with blinded subject IDs across all modules.
Absolutely. Import CDASH/CDISC-aligned forms or build from scratch with the no-code builder. Forms are reusable across studies.
Can we migrate an in-flight study?

Yes — we offer mid-study migration for EDC, eConsent, and ePRO replacements, including historic data import with audit trail preservation.

Yes — study designers can enable paper-to-source workflows for specific sites or regions when required by IRB/EC.
Data is frozen, a CDISC SDTM export is generated, and the full audit trail is preserved for retention windows you configure.

A platform built for the next decade of trials.

Book a 30-minute walkthrough with our clinical operations team and see ProCTTH configured for your protocol.