Water System Validation in Pharmaceutical Industry | GMP | IQ OQ PQ | WFI & PW Explained Part (2)
Автор: Qeema
Загружено: 2026-01-13
Просмотров: 184
In this video, we explain Water System Validation in the Pharmaceutical Industry, covering the key regulatory expectations, validation phases, and best practices in accordance with GMP, EU GMP Annex 1, and FDA guidelines.
You will learn:
✔ What is Pharmaceutical Water System Validation
✔ Types of pharmaceutical water (PW, WFI, Purified Water)
✔ Design qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ)
✔ Sampling strategies and microbiological monitoring
✔ Common validation mistakes and how to avoid them
✔ Regulatory expectations and inspection readiness
This video is ideal for:
🔹 Quality Assurance & Quality Control professionals
🔹 Validation & Engineering teams
🔹 Pharmaceutical production staff
🔹 Students and fresh graduates in pharma industry
📘 Presented by QEEMA – Pharmaceutical Consultation & Training
We specialize in GMP compliance, validation, and regulatory excellence.
📩 For training, consultation, or professional support, contact us or follow our channel for more expert content.
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