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 24, 2025
Standard Operating Procedure(SOP) Great! Here’s a suggested title and outline for the SOP (Standard Operating Procedure) for Operational Qualification (OQ) of a Dissolution Tester, followed by some hashtags you can use if...
by Dr. Yashashwini Reddy | Nov 24, 2024
Understanding Dirty Hold Time in Pharmaceutical Equipment Cleaning Dirty Hold Time (DHT) refers to the duration during which pharmaceutical equipment remains uncleaned after completing a manufacturing process. This period begins when the production ends and ends...
by Dr. Yashashwini Reddy | Oct 13, 2024
Y Chute in Compression Machines: A Key to Efficient Tablet Production In pharmaceutical tablet manufacturing, precision and efficiency are crucial. One important component that contributes to these factors is the Y chute, a device used to manage the flow of granules...
by Dr. Yashashwini Reddy | Sep 26, 2024
Understanding the Air Purge System in RMG: A Key to Pharmaceutical Safety In pharmaceutical manufacturing, maintaining cleanliness and preventing contamination is crucial. The air purge system in a Rapid Mixer Granulator (RMG) plays an essential role in ensuring...
