by Dr. Yashashwini Reddy | Apr 15, 2025
Sugar coating is when a layer of sugar or sucrose is applied over the core tablet, mainly to mask the taste. It’s the oldest technique used in pharmaceutical industries, and even though it’s a multistage and lengthy process, it’s been trusted for years....
by Dr. Yashashwini Reddy | Mar 30, 2025
Common Technical Document (CTD) for Regulatory Submission In the pharmaceutical industry, regulatory submissions are a crucial step in bringing new drugs to the market. One of the most widely accepted formats for regulatory submissions is the Common Technical Document...
by Dr. Yashashwini Reddy | Nov 28, 2024
Out of Specifications (OOS) in Pharmaceuticals Out of Specification (OOS) results occur when the test results of a pharmaceutical product fall outside the predefined acceptance criteria specified in regulatory guidelines or quality standards. These deviations are...
by Dr. Yashashwini Reddy | Nov 28, 2024
Why Data Integrity Matters in Pharmaceuticals: Insights from Patients and Regulators In pharmaceuticals, “data integrity” ensures data remains accurate, consistent, and reliable throughout its lifecycle. It forms the backbone of quality assurance in...
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...
