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Veeva QualityOne

Modern cloud for quality and compliance.

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Overview

Veeva QualityOne is a cloud-based quality management system (QMS) that is part of the broader Veeva Development Cloud for the life sciences industry. It provides a unified suite of applications for managing documents, training, quality events, and suppliers. QualityOne is designed to help life sciences companies streamline their quality processes and ensure compliance with global regulations.

✨ Key Features

  • CAPA Management
  • Document Control
  • Training Management
  • Change Control
  • Audit Management
  • Supplier Quality Management
  • Quality Risk Management

🎯 Key Differentiators

  • Part of the unified Veeva Development Cloud for life sciences
  • Modern, cloud-native platform
  • Strong focus on customer success and innovation

Unique Value: Veeva QualityOne provides a unified, cloud-based QMS that connects quality with other critical business processes, enabling life sciences companies to improve efficiency, collaboration, and compliance.

🎯 Use Cases (3)

Managing quality and compliance across the entire product lifecycle for life sciences companies Unifying quality management with regulatory, clinical, and other business processes Streamlining collaboration with suppliers and other external partners

✅ Best For

  • Integrated QMS for pharmaceutical, biotech, and medical device companies.

💡 Check With Vendor

Verify these considerations match your specific requirements:

  • Companies outside of the life sciences industry.

🏆 Alternatives

Sparta Systems MasterControl ETQ

Compared to standalone QMS solutions, Veeva QualityOne offers the advantage of being part of a broader platform that supports the entire product lifecycle, from clinical trials to commercialization.

💻 Platforms

Web iOS Android

🔌 Integrations

Veeva Vault Salesforce SAP

🛟 Support Options

  • ✓ Email Support
  • ✓ Live Chat
  • ✓ Phone Support
  • ✓ Dedicated Support (All plans tier)

🔒 Compliance & Security

✓ SOC 2 ✓ HIPAA ✓ BAA Available ✓ GDPR ✓ ISO 27001 ✓ SSO ✓ FDA 21 CFR Part 11 ✓ EU Annex 11 ✓ GxP

💰 Pricing

Contact for pricing
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