by Dr. Yashashwini Reddy | Aug 18, 2025
Sampling in Cleaning Validation in Pharmaceutical Industry Introduction Cleaning validation is a critical part of pharmaceutical manufacturing, ensuring that residues of products, cleaning agents, and microbial contaminants are effectively removed to avoid...
by Dr. Yashashwini Reddy | Aug 18, 2025
Recovery Factor Determination in Cleaning Validation Definition:Recovery Factor (RF) is the percentage of analyte recovered from a surface during cleaning validation studies. It helps to account for possible losses during swabbing/rinsing and analytical testing,...
by Dr. Yashashwini Reddy | Aug 18, 2025
Cleaning Validation of Pharmaceutical Equipment Cleaning Validation is a documented process that provides a high degree of assurance that equipment used in the manufacturing of pharmaceutical products is consistently cleaned to predetermined and acceptable limits. It...
by Dr. Yashashwini Reddy | Aug 10, 2025
Ultrasonic Cleaning for Equipment & Tooling: Overview How It Works Ultrasonic cleaning harnesses high-frequency sound waves—typically between 20–40 kHz—to create powerful micro-bubbles in a cleaning liquid. These bubbles implode (cavitation), generating intense...
by Dr. Yashashwini Reddy | May 15, 2025
Standard Operating Procedure (SOP) 1. Purpose To define the standard procedure for the operation, cleaning, and maintenance of the Cage Blender used for blending dry powders or granules to achieve a uniform mix. 2. Scope This SOP applies to...
