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 | Apr 27, 2025
Standard Operating Procedure (SOP) 1. Purpose This SOP outlines the procedure for cleaning the Disintegration Test Apparatus to ensure accurate and reproducible test results. Regular cleaning of the apparatus is essential to prevent contamination...
by Dr. Yashashwini Reddy | Apr 13, 2025
Solid Dosage Forms: Tablets Introduction: – Definition: Solid dosage form containing medicinal substances with or without suitable diluents. Common and widely used oral dosage form. Advantages: Convenient and portable Accurate...
by Dr. Yashashwini Reddy | Nov 27, 2024
Q1. What is disintegration, and why is it important in tablet evaluation? A: Disintegration is the process by which a tablet breaks down into smaller fragments in a liquid medium to release its active ingredients. It is important because proper disintegration is a...
by Dr. Yashashwini Reddy | Oct 21, 2024
The specifications of the disintegration test apparatus are crucial to ensure accurate and consistent results when evaluating the quality of immediate-release tablets. Each component and the movement of the apparatus are precisely designed to simulate conditions...
