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Verification and validation are independent procedures that are used together for checking that a product, service, or system meets requirements and specifications and that it fulfills its intended purpose. These are critical components of a quality management system such as ISO 9000.The words "
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Validation for the 21st Century series. U.S. Regulation 21 CFR 211.67 (b) (6) has required the "inspection of manufacturing equipment immediately before use" since 1979.
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Validation describes the procedures used to analyze pharmaceutical products so that the data generated will comply with the requirements of regulatory bodies of the US
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