
Veeva EDC
Collect, review, and process site-reported patient trial data with integrated quality controls and data management for clinical studies.
Overview
Veeva EDC is an electronic data capture system designed to support the full lifecycle of clinical trials, from study design through data lock and archiving. It is built for sponsors, CROs, and clinical data management teams running complex studies, including master protocols and adaptive trial designs. The platform has been available since 2016, has reached mature status, and is used by more than 100 customers, including eight of the top 20 biopharma companies.
Veeva EDC provides an end-to-end environment for collecting, reviewing, and processing site-reported patient trial data. It covers three main phases of a study: start-up, execution, and close-out, with dedicated capabilities at each stage.
Study Start-Up Capabilities
- Design of participant Case Report Forms (CRFs)
- Configuration of quality control checks
- In-product specification studio built on Agile Design principles for faster study builds
Study Execution Capabilities
- Collection of all patient form data
- Management of local lab data
- Medical coding
- Query management for data quality
- Targeted source data verification (SDV)
- Protocol deviation tracking
- Role-based user interfaces that prompt action to support SDV and medical assessments
- Support for complex trial designs, including master protocols and adaptive designs
Study Close-Out Capabilities
- Data lock functionality
- Post-processing features
- Automatic end-of-study media creation
- Automated archiving
Reported Performance Benchmarks
- Up to 50% faster study build times
- Complete elimination of known custom functions
- Study changes implemented up to nine times faster compared to prior approaches
Collaboration and Integration
- Veeva Connections enables data sharing and collaboration across the full study team
- Part of the broader Veeva Vault platform, which also includes CDB and eCOA
- Veeva eSource is an announced addition aimed at eliminating paper and streamlining data flow
Veeva EDC is positioned for organizations seeking to reduce build complexity and manual effort in clinical data management. Available resources include a features brief, white papers on agile EDC principles and custom function elimination, and a demo hub for hands-on evaluation.


