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What is Continuous Process Verification in Pharma about?

The document provides a comprehensive overview of Continuous Process Verification (CPV) in pharmaceutical manufacturing, emphasizing its role in ensuring consistent product quality throughout the lifecycle. It details the regulatory framework, Quality by Design (QbD) principles, and the importance of real-time monitoring and control strategies. Additionally, it outlines the stages of process validation, the tools and techniques used in CPV, and the significance of statistical process control in maintaining

Author

ch23b051

Language

EN