This video provides a complete GMP-oriented overview of Purified Water System Qualification in the pharmaceutical industry. It explains system components, water quality requirements, and the full DQ, IQ, OQ, and PQ lifecycle, with a clear, guideline-based explanation of PQ Phases I, II, and III. Regulatory expectations from FDA, EU GMP, WHO, ISPE, and USP 1231 are discussed along with sampling strategies, sanitization methods, documentation, deviations, and CAPA—ideal for QA, Engineering, and Validation professionals.
Refer to below link to access video on " WATER FOR PHARMACEUTICAL USE"
https://youtu.be/UjE6XGe10Yk?si=KCEJ5hd74oPm6PU4
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#PurifiedWaterSystem
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#PharmaTraining
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