The Validation Consultants team has served clients in the pharmaceutical, medical device and life sciences industries for more than 25 years, providing expert guidance and programs to ensure FDA regulatory compliance. We provide a full complement of CSV and auditing services dedicated to assuring conformance to 21 CFR Part 11, ISO 13485, QSR 21 CFR Part 820 and GxP best practices. 

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We provide the highest quality services, rapidly delivered at reasonable prices according to your schedule. We create and document repeatable processes and procedures that help you manage risk and comply with regulatory requirements.