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
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