by Dr. Yashashwini Reddy | Aug 8, 2025
Strategies for Resolving Stability Issues in Drug Formulations Stability issues can arise due to chemical degradation, physical changes, or microbial contamination, leading to reduced efficacy, altered safety, or shortened shelf life. The resolution process involves...
by Dr. Yashashwini Reddy | May 2, 2025
Preparation of Master Formula Record (MFR) in Pharmaceutical Manufacturing The Master Formula Record (MFR) is a critical document in pharmaceutical manufacturing. It serves as a detailed guide for producing a specific batch of a pharmaceutical product, ensuring that...
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 | Oct 5, 2024
Exploring the HLB Scale in Pharmaceuticals: Significance and Applications The Hydrophilic-Lipophilic Balance (HLB) system serves as an essential tool in pharmaceutical formulations, aiding in the selection of surfactants and emulsifiers for products such as lotions,...
by Dr. Yashashwini Reddy | Sep 30, 2024
Understanding Pre-formulation Studies in Pharmaceutical Drug Development What Are Pre-formulation Studies? Pre-formulation studies are a fundamental part of developing new pharmaceuticals. This process involves thoroughly investigating a drug’s physical and...
