Commissioning, Qualification & Validation (CQV)

DOC supports pharmaceutical and life science companies in ensuring that their facilities and equipment meet all regulatory, functional, and operational requirements — even before the system is installed.

Ensure compliance and performance from day one

At DOC, we offer end-to-end support for the Commissioning, Qualification, and Validation (CQV) of systems, utilities, and equipment within GMP-regulated environments. Our team combines strategic consulting with hands-on execution, ensuring that each validation activity — from early design to final performance verification — is fully compliant with regulatory expectations.

With extensive experience in the qualification of pharmaceutical systems, we help companies meet the requirements of FDA, EMA, and other international agencies. Our approach is grounded in ISPE Baseline Guide methodologies, enriched by a practical, solution-driven mindset that focuses on verifying all critical aspects of each system.