At Validation Solutions, we provide end-to-end CQV support across the full lifecycle of your equipment, utilities, cleanrooms, and GMP facilities. Our approach is risk-based, efficient, and grounded in scientific principles, ensuring each system is qualified from initial design through to routine operation. We guide you through every stage: confirming design suitability, verifying correct and traceable installation, challenging operational performance against defined parameters, and demonstrating consistent performance under real production conditions.
All CQV strategies are tailored to your processes and regulatory environment, aligned with FDA, EU GMP, WHO, and MHRA expectations. The outcome is a lean, inspection-ready programme that reduces delays and accelerates GMP readiness.