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The webinar will evaluate pharma GMPs and 21 CFR 58 and associated regulations to see how the GLPs can be implemented in the real world to achieve FDA requirements and ensure the accuracy and repeatability/reproducibility of lab results. It will further consider the USP 1058 requirements for lab equipment and analytic methods validations. There will be a detailed analysis of the applicable regulations for the industry. Register Now on conferencepanel.com, https://conferencepanel.com/conference/good-laboratory-practices-glp-and-usp-1058-validation
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