Veeva EDC

The Electronic Data Capture (EDC) system offers an end-to-end solution for gathering, reviewing, and processing site-reported data in clinical trials. During the initial stages of a study, it assists in designing patient forms and implementing quality control checks.

As the study progresses, EDC manages all data related to patient forms, local laboratory results, and medical coding. It incorporates quality control measures like querying, targeted source data verification (SDV), and monitoring protocol deviations. Upon study completion, EDC ensures data lock and supports post-processing activities, including automatic creation and archiving of study media.

Key Features

• Faster study builds by up to 50% through an in-product specification studio based on Agile Design principles.
• Elimination of known custom functions, enhancing efficiency.
• 9x faster implementation of study changes.

Benefits

• Cleaner data acquisition with minimal effort due to role-based user interfaces that prompt actions.
• Capability to run complex trials without experiencing downtime, accommodating master protocols and adaptive design needs.
• Seamless connection among clinical teams, enabling effective data sharing and collaboration across the study team.

Notably, prominent biopharma companies have transitioned to this EDC, such as eight out of the top 20 biopharmas. Success stories from industry leaders highlight the accelerated timelines and efficient processes achievable with this system.

The EDC system is recognized for significantly reducing the time needed for study build times and facilitating user acceptance testing (UAT) efficiently, even for complex trial designs.