by Dr. Yashashwini Reddy | Oct 9, 2025
Analytical procedure development is the process of designing and optimizing methods to accurately and precisely measure the active pharmaceutical ingredient (API), excipients, impurities, and degradation products in a drug substance or drug product. The goal is to...
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 | Nov 22, 2024
What is a Validation Protocol? A Complete Guide for the Pharmaceutical Industry In the pharmaceutical industry, achieving and maintaining high standards of quality is non-negotiable. A validation protocol is one of the critical tools that ensure processes, equipment,...
by Dr. Yashashwini Reddy | Nov 21, 2024
What is Analytical Validation? Why Is It Done? Analytical validation is a vital process in the pharmaceutical industry, ensuring the methods used for drug analysis are accurate, reliable, and consistent. By validating analytical methods, pharmaceutical companies...
by Dr. Yashashwini Reddy | Nov 21, 2024
Parts of Analytical Validation in the Pharmaceutical Industry Analytical validation plays a crucial role in ensuring that pharmaceutical products meet the highest standards of quality, safety, and effectiveness. It confirms that the methods used to analyze these...
