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 | Apr 28, 2025
Enhancing the stability of pharmaceutical formulations is a critical aspect of drug development and manufacturing. Stability ensures that the active ingredients in a drug maintain their potency, safety, and effectiveness throughout the product’s shelf life....
by Dr. Yashashwini Reddy | Apr 23, 2025
Standard Operating Procedure (SOP) Here is a Standard Operating Procedure (SOP) for the Operation and Calibration of Tablet Disintegration Apparatus. This SOP ensures that the apparatus used for testing tablet disintegration is operating...
by Dr. Yashashwini Reddy | Nov 25, 2024
Methods of Sterilization in the Pharmaceutical Industry Introduction Sterilization is a critical process in the pharmaceutical industry that eliminates microorganisms from products, equipment, and work environments. It ensures the safety, efficacy, and compliance of...
by Dr. Yashashwini Reddy | Nov 25, 2024
Forced Degradation Studies in Pharmaceuticals Introduction Forced degradation studies are essential in the pharmaceutical industry for evaluating the stability of drug substances and formulations. These studies involve exposing drugs to extreme environmental...
