Our CQV services are designed to ensure facilities and systems are audit-ready, fully compliant, and performance-proven from day one. Applying a risk-based approach aligned with ICH Q9 and the V-model lifecycle, we execute end-to-end qualification activities—covering DQ, IQ, OQ, and PQ—for all critical equipment and utilities. From URS development through protocol execution to final validation reporting, our team manages the complete CQV lifecycle in accordance with FDA, EMA, and SFDA standards. Emphasizing data integrity, traceability, and regulatory alignment, we help clients achieve seamless inspections and expedited market authorization.