CQV

Ensure regulatory compliance for pharmaceutical, biotech, and medical device facilities with our CQV services. We provide both routine equipment qualification (IQ/OQ/PQ) and large-scale facility validation, transitioning sites from construction to validated sterile GMP production. Our team takes over when facilities are ready for onsite commissioning and air balancing, ensuring equipment, utilities, and controlled environments meet FDA, EMA, and USP compliance standards.