Veeva QualityDocs
Streamline quality document control and GxP compliance.
Overview
Veeva QualityDocs provides a single source for all quality, manufacturing, validation, and other GxP documents and records. It helps life science companies manage the entire document lifecycle, from authoring and review to approval and distribution, while ensuring compliance with regulations like 21 CFR Part 11.
✨ Key Features
- Document Control
- Change Control
- Periodic Reviews
- Training Management
- Audit Trails
- Electronic Signatures
- Collaboration Tools
🎯 Key Differentiators
- Deep focus on the life sciences industry
- Part of the broader Veeva Vault platform
- Pre-validated for GxP compliance
Unique Value: A purpose-built, compliant solution for managing GxP content in the life sciences.
🎯 Use Cases (3)
✅ Best For
- Used by over 500 companies for managing GxP content.
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Organizations outside of the life sciences industry
🏆 Alternatives
Offers deeper life sciences industry expertise and a more comprehensive suite of applications compared to general-purpose document management systems.
💻 Platforms
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Varies by plan tier)
🔒 Compliance & Security
💰 Pricing
Free tier: NA
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