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PQ vs Process Validation Explained by Shady is a document available to read on EtoBox.

The document outlines the differences between Performance Qualification (PQ) and Process Validation in pharmaceutical manufacturing. PQ focuses on verifying the performance of specific equipment under real-world conditions, while Process Validation encompasses the entire manufacturing process to ensure product quality. Regulatory requirements from FDA, EU GMP, ICH, and WHO are also discussed, emphasizing the importance of both PQ and Process Validation in compliance and quality assurance.

Author
Shady
Language
EN