by Dr. Yashashwini Reddy | May 1, 2025
Standardization and Calibration of Dissolution Test Equipment is a critical aspect of pharmaceutical quality control. It ensures that drug dissolution tests are accurate, consistent, and compliant with regulatory standards such as those set by the United States...
by Dr. Yashashwini Reddy | May 1, 2025
Optimizing the Calibration Process for Dissolution Testing Equipment Dissolution testing is a crucial process in pharmaceutical and biopharmaceutical industries to ensure the release of active ingredients from solid dosage forms (e.g., tablets, capsules) into the...
by Dr. Yashashwini Reddy | May 1, 2025
Calibration of Disintegration Test Apparatus – Detailed Explanation The disintegration test apparatus is an essential quality control instrument used in the pharmaceutical industry to evaluate the time it takes for tablets or capsules to break down into smaller...
by Dr. Yashashwini Reddy | May 1, 2025
The calibration of volumetric glassware used in pharmaceuticals is crucial for ensuring accuracy and precision in the measurement of liquids. This is particularly important in the pharmaceutical industry, where even small variations in measurements can affect the...
by Dr. Yashashwini Reddy | Apr 29, 2025
Analysis of Out of Specification (OOS) Occurrences in Pharmaceutical Products In the pharmaceutical industry, the term Out of Specification (OOS) refers to situations where the results of tests or measurements fall outside the predefined limits or specifications set...
