Our CQV services bring your high‑tech facility into operation
Swiftly commencing manufacturing operations without delays is crucial in today’s fast‑paced industry landscape. CQV is essential for achieving this. Exyte supports clients by managing the complexities and compliance expectations that come with increasing automation, Industry 4.0 developments, and tightening regulations across advanced industries.
Our experience helps projects move from construction to operation without unnecessary interruptions. Through commissioning, qualification, and validation activities, our CQV teams help clients meet industry requirements, including cGMP and FDA regulations in the biopharma sector.
Supporting smooth transitions across all facility types
We also provide inventory documentation, process optimization, and upgrades that strengthen our clients’ competitive position while maintaining compliance. Every project has its own requirements, and our teams plan and execute CQV activities accordingly. From consulting and planning to final commissioning, we apply a careful, structured approach so that each facility is fully prepared for operation.
Benefit from Exyte's full range and combination of services
- Commissioning and start-up
- Qualification and validation
- As-built documentation
- Optimization, upgrades, and retrofits