Veeva QualityOne

The quality management application
that’s complete and easy-to-use

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Veeva Quality Summit 2018
Quality's Digital Transformation

June 5th, 2018 in Cincinnati, OH

Complimentary for quality professionals
and their IT partners from any industry

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Companies Succeed When
They Invest in Quality

See how Veeva can take you there


Quality is a strategic imperative across all companies and all job functions. QualityOne helps companies improve efficiency, visibility and control in quality management with a secure cloud solution that unifies processes, documents and data.

  • Bring together quality processes, document control, and data
  • Innovation that keeps pace and scales with your business
  • One application for employees, suppliers, and auditors
  • Just log-in and get to work
  • Access from any browser, any device, anywhere
  • High adoption improves compliance, visibility, and speed
  • Atomic Security provides total access control
  • Balance global standards and local autonomy
  • Validation made easy

Quality Management System


Document Control


Enterprise Content Management

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Cloud Application Development



What is Veeva QualityOne?


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Customers who trust Veeva

Hundreds of customers, from emerging companies to Fortune Global 500, trust Veeva to manage their most important processes, documents, and data.
“We run reports on a wide range of document lifecycle metrics across the enterprise, and are now able to anticipate potential bottlenecks or compliance risk well in advance.”
Cara Weyker | Vice President, CMC Regulatory and Quality, Horizon Pharma
“I knew we had to move to the cloud to optimize our resources. When we started our search, I wasn’t sure we could find a solution that would not require significant customization. It saves considerable time and resources.”
Kevin Loftus | Quality Assurance Manager, Medicines360
“With Vault, we’re able to find and view any document we need in seconds.”
Andy Katz, Ph.D., VP, Operations & Chief Business Officer, GeoMedX
“We’ve been able to harmonize globally on a single system so that processes and document templates can be standardized. This reduces the risk of making errors or duplicating efforts.”
Cara Weyker | Vice President, CMC Regulatory and Quality, Horizon Pharma