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What is Master Validation Plan for Liquids & Semi-Solids about?

This document presents the Master Validation Plan for non-sterile liquid and semi-solid pharmaceutical forms of a laboratory. It describes the validation strategy, which includes the qualification of areas, systems, and equipment, as well as the validation of production processes, packaging, and cleaning. The objective is to verify that the processes are consistent and reproducible, and that the final product meets the quality attributes.

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ScribdTranslations

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EN