by Dr. Yashashwini Reddy | May 3, 2025
Granule size plays a crucial role in the formulation and performance of tablet-based pharmaceutical products. It significantly affects both the stability of the tablet during its shelf life and the bioavailability of the drug when taken by the patient....
by Dr. Yashashwini Reddy | May 1, 2025
Quality by Design (QbD) in Pharmaceuticals: A Detailed Explanation Quality by Design (QbD) is a systematic approach to pharmaceutical development that aims to ensure the quality of a drug product through the design and control of the manufacturing process. This...
by Dr. Yashashwini Reddy | Nov 13, 2024
In the world of pharmaceuticals, Active Pharmaceutical Ingredients (APIs) and Intermediates are essential yet distinct parts of the drug manufacturing process. Understanding Active Pharmaceutical Ingredients (APIs) An API is the core component of a drug, directly...
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...
by Dr. Yashashwini Reddy | Jul 18, 2024
What is BCS classification? According to the BCS classification system, drugs are classified based on their solubility and intestinal permeability. The full form of BCS is the Biopharmaceutics Classification System. Drugs are classified by considering their...
