COMISSIONING, QUALIFICATION AND VALIDATION (CQV)

Commissioning, Qualification and Validation (CQV)

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.

How can we support your business?

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.

Stepwise’s CQV services includes:

  • Commissioning of facilities, utilities and equipment;
  • Qualification and Validation (Q&V) of facilities, utilities, equipment and computerized systems;
  • Support to Process Validation activities;
  • Support to Analytical Methods Validation activities;
  • Support to Cleaning Validation activities;

check all stepwise services here

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