We provide CSV expertise in the validation requirements of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Good Clinical Practices (GCP) systems to comply with FDA regulations. Our validation professionals will document the quality, accuracy and consistency of your systems, methods and processes, either following your existing validation procedures or helping you create compliant procedures and processes.

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We help FDA-regulated businesses document and implement repeatable  processes that comply with exacting validation requirements for computer system software and process & equipment.

 

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