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Structured services for validating, qualifying, and commissioning equipment, systems, and processes in compliance.
Our Commissioning, Qualification, and Validation (CQV) services are designed to ensure that your equipment, facilities, and processes meet the necessary regulatory requirements.
From installation qualification (IQ) to performance qualification (PQ), we provide a structured, risk-based approach to validation. Our expert team works closely with you to guarantee that all systems and operations are compliant with GMP, FDA, and EMEA standards.
By streamlining validation procedures, we help you achieve operational efficiency and maintain the highest standards of quality.
We offer customized commissioning, qualification, and validation strategies that align with your business objectives and regulatory demands.
Whether you need full project management or specific validation tasks, we ensure that all steps are documented in accordance with industry standards. Our team handles everything from process validation to equipment testing and on-site validation support.
With over 14 years of experience, we have helped leading pharma companies maintain compliance and improve their operational efficiency through effective CQV services.
Take the first step towards seamless validation, qualification, and compliance today. Our expert team is here to guide you through every phase of your project, ensuring efficiency and regulatory adherence.
Contact us now to discuss your CQV needs and receive customized solutions tailored to your business!
Pharma & biotech compliance experts
GMP, FDA, and EMEA certified
Custom strategies for every project
14+ years of industry success
With our comprehensive approach to commissioning and validation, we ensure that your systems and equipment operate as intended, safely, and within specified limits.
Our validation process is tailored to each project, addressing your unique needs while maintaining industry compliance. We handle the entire validation lifecycle, including the creation of validation plans, execution, and ongoing maintenance.
By working with CPH Pharma, you can be confident that your validation processes will meet all regulatory standards, minimize risk, and optimize efficiency.
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