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Expert Computer System Validation Services

Our CSV practice provides GAMP 5-compliant validation services for pharmaceutical and biotech companies. Whether you need a gap assessment, full system validation, or enterprise CSV program development, we bring decades of industry experience to your compliance needs.

CSV Assessment & Roadmap
Understand your validation gaps before your next audit. 2-3 week assessment with prioritized remediation roadmap.
System Validation Execution
Complete IQ/OQ/PQ validation for critical GxP systems. Full documentation package ready for FDA inspection.
CSV Program Development
Build internal validation capability with SOPs, templates, and training. Scale your compliance operations efficiently.

Computer System Validation Services

Why IntuitionLabs for CSV?

Our validation team combines deep pharma quality operations experience with modern systems expertise. We understand both the regulatory requirements and the practical realities of implementing compliant systems.

Industry Experience

23 years at Pfizer Quality Operations, 13 years at Veeva Systems, 65+ site deployments across global pharmaceutical manufacturing.

Modern Systems Focus

Expert validation of cloud/SaaS platforms, Veeva Vault (QMS, RIM, CTMS), LIMS/ELN, and AI/ML systems in GxP environments.

Practical Approach

Risk-based methodology per GAMP 5 Second Edition. Inspection-ready documentation without unnecessary bureaucracy.


Learn More About Our CSV Services

IntuitionLabs Validation Team