CQV: From design to a fully qualified facility

Progress is your partner for Commissioning, Qualification and Validation (CQV) throughout all project phases in the (bio-)pharmaceutical and healthcare industry. We help ensure your facility, utilities, systems and equipment meet regulatory and business requirements — from design and construction through to a fully qualified and validated state, ready for GMP operations.

How can we help you?

We can support your new or existing facility by managing or executing the full CQV scope, including risk-based qualification strategies, validation of utilities and equipment, process validation, cleaning validation, and computer system validation — always aligned with the latest regulatory expectations and industry best practices.