Eric Electronic Data Capture(EDC)
Capture and Re-use Research Data from anywhere and anytime
ERIC’s Electronic Data Capture (EDC) simplifies the process of capturing your trial data and integrating it seamlessly with other data in your clinical trial ecosystem. ERIC EDC offers one of the shortest build times, with more than 90% of our studies deployed within the first three weeks.
Explore ERIC EDC, our most robust module, to see how it can help you capture and manage all your study data in one centralized hub. If your needs extend further, easily incorporate ERIC eConsent and ePRO to build a comprehensive ecosystem of research tools.
Capture and Re-use Research Data from anywhere and anytime
Explore ERIC EDC, our most robust module, to see how it can help you capture and manage all your study data in one centralized hub. If your needs extend further, easily incorporate ERIC eConsent and ePRO to build a comprehensive ecosystem of research tools.
Deploy Studies Faster
Deploy Studies Faster
- Create advanced eCRFs in minutes.
- Deploy your study in as little as 3 weeks.
- Manage study complexities with best-in-class support.
Decentralized Data Integration
Decentralized Data Integration
- Integrate data from EHR, eCRF, ePRO/eCOA, laboratory, wearables, and other devices.
- Integrate with any software or database in your clinical trial ecosystem using ERIC’s open API.
Real-Time Visibility
Real-Time Visibility
- Get an overview of study statistics as your studies are ongoing.
- Track data entry progress and outstanding queries.
- View verification status (SDV) for steps.
- ERIC introduces enhanced analytical dashboards.
Acheive Global Compliance Easily
Acheive Global Compliance Easily
- Comply with global standards 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.
- Adhere to GCP, HL7 FHIR, and other regulatory guidelines.
Features
Build Advance eCRF quickly
Build Advance eCRF quickly
- Begin with one of our pre-built eCRF templates.
- Customize your form with 21 different field types.
- Clone and reuse forms as you develop additional studies
Store Data Securely
Store Data Securely
- Store study data in real-time.
- Store it automatically on certified, compliant servers in any country.
- Safeguard your data with 25-year retention, field-level encryption, and two-factor authentication.
Amend Studies With Less Risk
Amend Studies With Less Risk
- Simplify protocol amendments with a tool that’s secure, trackable, and easy to validate.
- Easily create test environments for your subsequent studies.
Acheive Global Compliance Easily
Acheive Global Compliance Easily
- Comply with global standards 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.
- Adhere to GCP, HL7 FHIR, and other regulatory guidelines.
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