Veeva DQS
Automate and Centralize Clinical Data Workflows
Veeva DQS is a Data Quality System that provides a central environment to manage all trial data, automate workflows, and orchestrate review across the clinical ecosystem. The system automatically aggregates, reconciles, and cleans data from multiple sources—including EDCs, RTSM, eCOA, labs, imaging, and more—to provide a harmonized data package for downstream use.
Data managers use DQS to create and manage queries, protocol deviations, and communications with data providers across all sources. The system automates data actions, including change detection and the creation or closure of queries and protocol deviations. Cross-functional teams collaborate on data review in real-time, while oversight teams monitor study health via interactive dashboards.
Announced 2018 Status Mature Customers51-100
Survival of The Fastest: A Practical Framework for Risk-Based Data Management
Impact
Deliver quality data faster
75%
faster external data ingestion
90%
less effort for manual queries
50%
faster last subject last visit (LSLV) to database lock
Why Veeva DQS
Automate 50% of manual effort
Customer Success
Trusted by 8 top 20 biopharmas and 3 top 10 global CROs
Resources
Explore and Learn
Watch Customer Story
Boehringer Ingelheim Boosts Efficiency and Oversight with Veeva DQS

Read Features Brief
Veeva DQS Features Brief

Read White Paper
Survival of the Fastest: A Practical Framework for Risk-Based Data Management

Read Customer Story
How GSK Cut Time to Database Lock by 50%

Read Press Release
Veeva Clinical Database Crosses 200 Study Milestone

Read Customer Story
Syneos Health Transforms Clinical Data Management

Learn More
Innovating Clinical Data with AI, eSource, and RBQM

Read Report
A Blueprint for Clinical Trial Transformation: Results from Three Top 20 Biopharmas

Watch Video
Veeva DQS Features Highlights – April 2026
