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Standard Guide for Application of Continuous Process Verification to Pharmaceutical and Biopharmaceutical Manufacturing Ingestion-build-105964 Categories and their relation to1. Scope 1. 1 This guide describes Continuous Process Verification as an alternate approach to process validation where manufacturing process (or supporting utility system) performance is continuously monitored, evaluated, and adjusted (as necessary). It is a science based approach to verify that a process is capable and will consistently produce product meeting its predetermined critical quality attributes. Continuous Process Verification (ICH Q8) is