Master Cleaning Validation: Analytical Method Requirements & Parameters (
Автор: The Indian Pharmacist
Загружено: 2026-01-05
Просмотров: 108
In this video, we dive deep into the essential requirements of Analytical Method Validation specifically for Cleaning Validation in the pharmaceutical industry.
Many professionals confuse general method validation with cleaning validation requirements. We explain the key differences and why parameters like LOD, LOQ, and Swab Recovery are critical for regulatory compliance.
What you will learn in this video:
✅ Difference between Specific and Non-Specific Analysis [01:44]
✅ Importance of LOD & LOQ (Limit of Detection/Quantification) [02:38]
✅ Why Linearity and Specificity matter [06:26]
✅ Accuracy vs. Precision in Cleaning Validation [09:28]
✅ Sample Hold Time & Filter Compatibility [12:53]
✅ Swab Recovery & Surface Evaluation (SS, Glass, Polymeric) [17:01]
If you are a Pharmacy student or working in QA/QC, this video is a must-watch!
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