CQV (Commissioning, Qualification, and Validation) is a very detail-oriented process that requires the right mix of knowledge, experience, and diligence to correctly place equipment/systems into use.
Additionally, with global medicinal authorities’ regulations and requirements continually changing, it is crucial to understand the CQV lifecycle to remain compliant.
Our dedicated CQV engineers bring wide-and-deep knowledge of the entire validation lifecycle to support all major sectors within the Pharmaceutical and Life Sciences industry. We guide you in the selection of the right validation strategy and fully support all your tactical, hands-on deliverables, from protocol preparation, through “floor executions” and data analysis.
Stepscience’s CQV services includes: