The operating system for modern clinical trials.
ProCTTH unifies eSource, eCRF, and patient engagement into one ‘site-centric clinical research’ operating system designed to digitalize clinical studies into hybrid and decentralized studies.
No-code
Site-first
Blinded eSource
data view
Zero Setup Fee
self onboarding
- Our vision
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.
- The Proctthify Network
Sites that run on ProCTTH are Proctthified
Proctthify sites are certified, site-centric clinical research centers running paperless eSource, engaging subjects through ProCoins, and delivering blinded, audit-ready data to sponsors in real time.
Proctthify Site
- Three platforms · One system
One source of truth, three points of view. .
ProCTTH is built on a unified data model with role-aware experiences for every stakeholder in a trial, from the bedside to the boardroom.
For Clinical Sites
Use ProCTTH as eSource. Capture data once, eliminate transcription, and engage subjects between visits with chat, video, and ProCoins.
For Sponsors & CROs
A real-time eCRF with audit-ready data, blinded by design. Subject identity never leaves the site, and CRAs monitor remotely.
For Subjects
Discover trials, e-consent, complete visit forms, connect wearbale devices, and earn ProCoins for milestones all from one app.
- Study Setup
Launch a study without writing code.
Drag-and-drop visit form builder. Calendar-view schedule of assessments. Conditional logic, validations, and edit checks; all configured by your team in hours, not months.
- Visual schedule of visits with calendar
- Drag & drop form builder with 30+ field types
- Conditional branching, edit checks, derivations
- Versioned study amendments with audit trail
- Reusable form across studies
- How it works
Set up your study schedule, visits, and visit forms quickly and efficiently.
- 01
Design
Refine forms, edit checks, and roles in the no-code builder. Publish in one click.
- 02
Configure
AI training system to assist in data discrepancy identification in forms
- 03
Run
Sites enroll, subjects engage from the app, and data flows into eSource and the blinded eCRF live.
- 04
Lock
Real-time queries and eSDV mean clean data at the end of the study, not weeks after.
- Capabilities
Everything a modern trial needs, in one platform.
Study Matching
Subjects are matched to eligible studies using subject app profile, and inclusion criteria.
Wearables
Smartwatches help capture subject vitals for clinical study monitoring.
Lab Visit Scheduling
Subjects choose home or on-site visits; sites see readiness in real time.
Web Call & Chat
Secure video calls between subjects and investigators, with dedicated chat between subjects and CRCs, and between investigators, CRCs, and CRAs.
Notifications
Configure notifications and send manual or emergency notifications across study roles.
ProCoins Engagement
Reward subjects for milestone completion; driving retention and adherence.
Identity Blinding
Subject identity is never exposed to CRAs, CROs, or sponsors. Privacy by design.
Mobile-First
Native apps for subjects, investigators, and CRAs built for decentralized trials.
Behavior Monitoring
ML-powered subject engagement analytics to predict drop-off before it happens.
- Mobile-First Trials
The trial fits in their pocket. .
- Subjects join studies, e-consent, complete visit forms, stream IoT data, and chat with their investigator, all from one app. Investigators, CRCs and CRAs get matching apps tuned to their roles.
Capabilities & Intelligence
Next-Gen Power for Modern Clinical Trials.
Conventional EDC System
- Electronic Capture of Clinical Data
- eCRF/Data Collection
- Source Document entered eCRF
- Limited
- Separate System or Integration
- Limited, Requires Multigrations
- Email/Phone/External Tools
- External Systems
- Not Available
- Separate Integrations
- Standard Edit Checks and Queries
- Form/Database Configuration
- Multiple Specialized Systems
- Traditional Site-based Trials
- Better Electronic Data Collection
ProCTTH
- Site-Centric Trial Operating System
- Site-Patient-Investigator-Sponsor
- eSource + eCRF
- Patient App, eDiary, Notifications
- Integrated eConsent
- Hybrid and DCT Ready
- Connected Site-to-patient Workflows
- Integrated Remote Activities
- Randomize after eConsent
- Smartwatch/ Wearables Connectivity
- AI + OCR for Discrepancy Detection
- No-code/ Low-code Study Setup
- One Platform; Fewer Systems
- Traditional + Hybrid + Decentralized
- Better Study, Patient Engagement, Site Efficiency, and Data Quality
- What teams are saying
Loved by sites, trusted by sponsors.
“We replaced three tools with ProCTTH. Site coordinators stopped complaining within a week.”
Dr. M. Patel
Principal Investigator, Oncology
“Our CRAs review remotely. Monitoring time dropped by half.”
S. Lindqvist
Head of Clinical Operations, mid-size CRO
J. Romero
Study Manager, Cardiovascular Sponsor
- Plays well with others
Native integrations across your research stack.
EDC
CTMS
EHR
Lab vendors
ePRO
Identity
Storage
Analytics
- DCT Platform
One Platform. Multiple Stakeholders.
Participants, investigators, CRCs, and CRAs work within one connected platform, with each stakeholder getting the tools and workflows tailored to their role. From e-consent and visit forms to monitoring, data review, and participant engagement, everyone stays connected through a shared clinical trial ecosystem.
- Why Proctthify sites lead
Built for sites. Loved by sponsors.
Joining the Proctthify Network means your site runs on the same operating system trusted by CROs and sponsors with measurable gains from day one.
Better communication driving better adherence and fewer subject dropouts.
- Ready when you are