by Dr. Yashashwini Reddy | Nov 1, 2024
Understanding Why-Why Analysis in Pharmaceuticals: Uncovering the Root of Quality Issues The Why-Why analysis, or “5 Whys,” is a structured root cause analysis method widely used in the pharmaceutical industry to identify and resolve issues at their...
by Dr. Yashashwini Reddy | Nov 1, 2024
Importance of Critical Process Parameters (CPPs) in Pharmaceutical Manufacturing Critical Process Parameters (CPPs) are key to ensuring product quality in the pharmaceutical industry. These parameters—such as temperature, pH, mixing speed, and pressure—are closely...
by Dr. Yashashwini Reddy | Nov 1, 2024
Understanding the Difference Between Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs) in Pharmaceuticals In pharmaceutical manufacturing, maintaining high product quality is essential, and two important concepts—Critical Quality Attributes...
by Dr. Yashashwini Reddy | Nov 1, 2024
Disinfectant Validation in the Pharmaceutical Industry In the highly regulated world of pharmaceuticals, maintaining clean and sterile environments is essential to ensure product safety and quality. Disinfectant validation plays a critical role in this process,...
by Dr. Yashashwini Reddy | Oct 24, 2024
Good Laboratory Practices (GLP) in the pharmaceutical industry are a set of internationally recognized standards that ensure the quality, consistency, and integrity of non-clinical studies. These practices are critical for ensuring that the data generated during drug...
