Electronic Data Capture
TrialBridge's electronic data capture (EDC) makes it easier to capture your trial data and integrate it seamlessly with other data in your clinical trial ecosystem. TrialBridge ranks among the top 5% of EDC's for shortest build time, with more than 90% of our studies being deployed within the first 4 weeks.
Capture and re-use research data from anywhere, anytime.
Explore TrialBridge EDC/CDMS, our most robust module, and how it can help you capture and manage all your study data in one centralized hub. And if your needs go beyond, easily layer in eConsent and ePRO to build a full ecosystem of research tools.
Deploy studies faster
TrialBridge is designed with usability in-mind for all, regardless of technical expertise.
Build advanced eCRFs in minutes
Start with pre-built templates and customize with 21 different field types.
Deploy your study in as little as 4 weeks
90% of our studies are deployed within the first 4 weeks.
Navigate study complexities with ease
Best-in-class support for all technical expertise levels.
Create better data flow
Connect and manage all trial components and integrations, in one place.
- Integrate data from EHR, eCRF, ePRO/eCOA, laboratory, wearables, and other devices
- Work with any software or database in your clinical trial ecosystem with TrialBridge's open API
Gain real-time visibility
Monitor study progress and outcomes in real-time with TrialBridge's study health dashboard.
- Get an overview of study statistics as your studies are ongoing
- Track record data entry progress and outstanding queries
- View Verification Status (SDV) for Steps
Generate compliant data, confidently
Build advanced eCRFs in minutes
- Start with one of our pre-built eCRF templates
- Customize your form with 21 different field types
- Clone and re-use forms as you build more studies
Store data securely
- Save study data in real-time
- Store it automatically on certified, compliant servers in any country
- Protect your data with 25-year data retention, field-level encryption, and two-factor authentication
Amend studies with less risk
- Simplify protocol amendments by using a tool that's secure, trackable, and easy-to-validate
- Easily create test environments for each of your subsequent studies
Achieve global compliance
- Meet compliance certifications worldwide such as FDA CFR Part 11, GDPR (EU), ICH GCP (HIPAA, US), ISO 27001, and ISO 9001
- Align with GCP, HL7 FHIR, and other regulatory guidelines
Analysts respect us
Clinical trials succeed when data flows. That's why TrialBridge is reengineering traditionally stodgy processes with easy-to-use digital tools that remove barriers for participants and researchers.
Explore how we can bridge the gap from siloed, cumbersome clinical trial processes to fully connected, interoperable clinical trial platforms for collecting and analyzing data.
Ready to accelerate your trials?
Deploy your study in as little as 4 weeks with TrialBridge EDC.