Integrated by design
Use the modules your study needs while keeping data and workflows connected across the platform.
GROUP← THEO SOLUTIONS
CLINICAL TRIAL DATA PLATFORM
eCRFast
Capture the data. Connect the trial. Move research forward.
ONE CONNECTED TRIAL PLATFORM
From first data point to study oversight.
eCRFast by THEO brings essential clinical-trial applications into a flexible, integrated environment. Study teams can capture and review data, engage participants, manage randomization and coordinate investigational product workflows without losing sight of the complete trial.
Configured for the protocol
Adapt study forms, participant pathways, randomization and operational controls to the requirements of each trial.
Data visible in real time
Give authorized study teams timely access to the information needed to monitor progress and act on issues.
MODULAR CAPABILITIES
The tools every modern trial needs.
A connected suite spanning clinical data capture, participant engagement, randomization and study-product workflows.
Electronic Data Capture
Design study-specific electronic case report forms, capture clinical data and support validation, review and query workflows in real time.
Electronic Patient-Reported Outcomes
Give participants a clear digital pathway to complete questionnaires and report outcomes on schedule, wherever the study requires.
Interactive Web Randomization
Centralize participant randomization with real-time assignment visibility and study-controlled allocation workflows.
Electronic Source
Capture source data digitally at the point of research activity and reduce unnecessary transcription between disconnected systems.
Electronic Consent
Support informed-consent workflows with accessible digital experiences, controlled documentation and study visibility.
Investigational Product Management
Coordinate product allocation and distribution alongside randomization to create a more unified trial workflow.
BEYOND THE PLATFORM
Clinical data expertise, built around your study.
Study configuration
Database design, eCRF development, edit checks and study-specific workflow configuration.
Data management
Data review, cleaning, query support and operational coordination throughout the study lifecycle.
Analytics & applications
Reporting, trial insight, custom clinical applications and integration with the systems your study relies on.
DESIGN THE RIGHT STUDY ENVIRONMENT
Start with your protocol and data needs.
Tell us about your study, participant journey and operational requirements. We’ll focus the conversation on the eCRFast modules and services that fit your trial.
Request an eCRFast conversation ↗