Ensure Compliance and Data Integrity with Agilent Computer System Validation Services

Agilent CrossLab computer system validation (CSV) is the foundation for data integrity compliance, which is the main focus of regulatory audits and warning letters issued by the FDA. Our experts can help assess your overall risk, streamline validation by focusing on high-risk areas, and comply with regulatory guidelines and regulations.

Validation is a lifecycle process that includes new system commissioning, change control for system upgrades/relocations, and decommissioning systems for archival. Agilent supports your lab every step of the way with these CSV services. Partner with us for efficient and cost-effective validation. Agilent Technologies can assist our customers through all phases of the validation life cycle: Requirements Gathering, Risk Assessment, Validation and Training, Change Management consulting, and System Retirement.


  • Support for every step of the validation lifecycle, including system commissioning and decommissioning and change control for upgrades or relocations
  • Effectively evaluates compliance risk to meet data integrity requirements
  • Improves efficiency of validation by considering high-risk areas and intended use

Download to know more.

    This is co-hosted by Express Pharma and Agilent

    By submitting this form, you are confirming you are an adult 18 years or older and agree to Express Pharma contacting you with marketing-related emails or by telephone. You may unsubscribe from receiving such communications from Express Pharma at any time. Express Pharma web sites and communications are subject to our Privacy Notice and Terms of Use.

    Yes, I would like to receive email updates about Agilent products, services and events.
    For full details of how we will treat your information please view our privacy policy: www.agilent.com/home/privacy-policy

    Comments (0)
    Add Comment