Validate with Confidence. Stay Audit Ready.
VALID is the modern validation management platform built for life sciences companies to streamline GxP validation, ensure compliance, and reduce risk.
Validation Dashboard
Projects
24
In-Progress
8
Completed
16
Overdue
2
Validation Status
Recent Activity
Khalid H. Approved OQ Protocol
Sofia M. Submitted IQ evidence
John S. Review pending — VAL-003
Trusted by Life Sciences Leaders
Everything You Need to Validate Smarter
Powerful features built for validation teams.
Validation Planning
Create risk-based plans faster with templates, workflows and reuse.
Execution & Evidence
Capture, organize and link evidence in one place. Keep everything traceable.
Review & Approval
Streamline reviews with electronic approvals and audit trails.
Change Control
Manage changes, assess impact and maintain compliance.
Reports & Insights
Real-time dashboards and reports to keep you inspection ready.
How VALID Works
A simple, modern approach to validation management.
Plan
Create your validation plan with templates and define scope.
Execute
Collect evidence, track tasks and manage execution.
Review & Close
Review, approve and close with complete audit trail.
Built for Compliance. Backed by Security.
VALID helps you meet the highest regulatory and security standards.
Loved by Validation Teams
“VALID transformed our validation process. We went from spreadsheets to a fully audit-ready system in weeks. Our last FDA inspection had zero CSV findings.”
Director of Validation
Top 10 Pharma Company
“The electronic signature workflows and audit trails give us complete confidence. Our QA team can review and approve protocols in half the time.”
Head of Quality Assurance
Global Biotech Leader
“Finally, a platform built by people who understand GxP. The V-Model lifecycle support and traceability matrix are exactly what we needed.”
CSV Consultant
CSV Consulting LLC
Simple, Transparent Pricing
Choose the plan that fits your organization.
Essentials
For small validation teams getting started.
Up to 5 users
- Validation project management
- Document templates & authoring
- Basic electronic signatures
- Audit trail export
Professional
For growing organizations with complex needs.
Up to 20 users
- Everything in Essentials, plus
- Full V-Model lifecycle
- Protocol execution & evidence
- Regulatory checklists & gap analysis
- AI assistant (Ana)
Enterprise
For large organizations with advanced requirements.
Unlimited users
- Everything in Professional, plus
- SSO / SAML integration
- Dedicated success manager
- Custom workflows & integrations
- SLA & priority support
Frequently Asked Questions
Yes. VALID is designed from the ground up to meet FDA 21 CFR Part 11 requirements, including unique user identification, electronic signature manifestations, audit trails, and record retention. Our platform undergoes continuous validation to maintain compliance.