by Dr. Yashashwini Reddy | May 3, 2025
Identifying and Preventing Tablet Defects in Pharmaceutical Manufacturing Processes:- Tablet manufacturing is a complex process that requires precision, consistency, and stringent quality control to produce high-quality pharmaceutical tablets. Tablet defects can...
by Dr. Yashashwini Reddy | May 2, 2025
Equipment malfunction in pharmaceutical production can have wide-ranging and serious implications, affecting not only operational efficiency but also regulatory compliance, product quality, and patient safety. Here’s a detailed explanation of how such malfunctions can...
by Dr. Yashashwini Reddy | Apr 30, 2025
The practice of calibrating dissolution testers with salicylic acid tablets was discontinued for several reasons: Inconsistent Results: Salicylic acid tablets showed variations in their dissolution profiles, which could result in inconsistent and unreliable...
by Dr. Yashashwini Reddy | Apr 29, 2025
The essential GMP (Good Manufacturing Practice) compliance requirements for pharmaceuticals are designed to ensure the consistent production of high-quality, safe, and effective medicinal products. These requirements are globally recognized and enforced by regulatory...
by Dr. Yashashwini Reddy | Apr 28, 2025
Resolving API Impurity Issues in Drug Development:- In pharmaceutical drug development, Active Pharmaceutical Ingredients (APIs) are the core components responsible for the therapeutic effect of a drug. However, during the manufacturing and synthesis of APIs,...
