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Veeva Vault QMS

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Pharmaceutical quality management on the platform the regulated documents already live on

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Veeva Vault QMS screenshot See all screenshots
  • Deployment Cloud Based, SaaS
  • Starting price Not published
  • Free trial Not offered
  • Best for Medium Business, Large Enterprise

What is Veeva Vault QMS?

Veeva Vault QMS is a quality management system for life sciences, part of Veeva's Vault platform alongside clinical products including eTMF and CTMS, with coverage extending to MedTech, consumer packaged goods, food and beverage and chemical industries across North America, Europe, China, Japan, Asia Pacific and Latin America.

Running on the same platform as the regulated documents is the argument for Vault QMS specifically, and in this industry it is a strong one. A deviation investigation references batch records, standard operating procedures and training records, and when those live in a separate document system the investigation becomes an exercise in cross-referencing that an inspector will probe.

Life sciences quality management is a distinct discipline rather than a configuration of general QMS, because the regulator can inspect the system itself, validation of the software is a deliverable, and electronic signatures carry legal weight under specific rules that general quality software does not attempt.

Extending into MedTech, consumer goods, food and beverage and chemicals is a sensible widening, since those industries face comparable if less onerous regimes and Veeva can carry the same rigour into them without rebuilding. Veeva publishes in six regional configurations. Rates are not published.

Key Features of Veeva Vault QMS

  • Quality management for life sciences
  • Deviation and investigation management
  • Corrective and preventive action
  • Change control
  • Complaint handling
  • Audit management
  • Quality event tracking
  • Built on the Veeva Vault platform
  • Shared platform with regulated documents
  • Validation and electronic signature support
  • MedTech, CPG, food and chemical coverage
  • Regional configurations across six markets

Veeva Vault QMS Pricing

Not published

Not published

No rate is published. Veeva quotes per organisation on users, products licensed and validation scope.

Veeva Vault QMS Specifications

Deployment
  • Cloud Based
  • SaaS
Desktop
  • Web App
Mobile
  • iOS
  • Android
Built for
  • Medium Business
  • Large Enterprise
Support
  • Email
  • Phone
  • Knowledge Base
Public API
Yes
Free trial
No
Free plan
No
Runs in browser
No
Customisable
No
Website
veeva.com

Veeva Vault QMS Videos

Veeva Vault QMS Screenshots

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Veeva Vault QMS FAQs

Rates are not published. Veeva quotes per organisation on users, products licensed and validation scope, with sales contact published.

A deviation investigation references batch records, procedures and training records. When those live in a separate document system the investigation becomes cross-referencing that an inspector will probe.

The regulator can inspect the system itself, validation of the software is a deliverable, and electronic signatures carry legal weight under specific rules that general quality software does not attempt.

MedTech, consumer packaged goods, food and beverage and chemical, which face comparable if less onerous regimes.

Clinical products including Veeva eTMF for trial master files and Veeva CTMS for trial management, within the wider Veeva Development Cloud.