Clinicalveda’s Electronic Data Capture
clinicalveda Solutions offers Regulatory and GDPR compliant technologies with GenAI enhancements.
Clinicalveda’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. clinicalveda EDC has one of the shortest build time, with more than 90% of our studies being deployed within the first 3 weeks.
Capture and Re-use Research Data from anywhere and anytime
Explore clinicalveda EDC, 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 clinicalveda eConsent and ePRO to build a full ecosystem of research tools.
clinicalveda EDC is designed with usability in-mind for all, regardless of technical expertise.
- Build advanced eCRFs in minutes.
- Deploy your study in as little as 3 weeks.
- Navigate study complexities with best-in-class support.
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 Clinicalveda’s open API
Monitor study progress and outcomes in real-time with Clinicalveda’s study health dashboard and Customized Reports
- 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
- clinicalveda introduces enhanced analytical dashboards
Features of clinicalveda EDC
- 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.
- 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.
- 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.
- Meet compliance requirements 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
- class="text-bold">Align with GCP, HL7 FHIR, and other regulatory guidelines