by Dr. Yashashwini Reddy | Oct 27, 2024
Ensuring Quality in Tablet Manufacturing: The Essential Role of Critical Quality Attributes (CQAs) Introduction In the pharmaceutical industry, ensuring the consistent quality, safety, and effectiveness of products is non-negotiable. Tablets, one of the most common...
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 | Oct 18, 2024
Understanding the Difference Between Out of Trend (OOT) and Out of Specification (OOS) in Pharmaceuticals In the pharmaceutical industry, maintaining product quality and regulatory compliance is critical. Two key terms often encountered in quality control are Out of...
by Dr. Yashashwini Reddy | Oct 15, 2024
Standard Operating Procedure (SOP) for Prevention of Mix-up in the Dispensing Area 1.0 Objective This SOP outlines the steps and measures required to prevent mix-ups and ensure proper control in the dispensing area during operations. 2.0 Scope This procedure is...
by Dr. Yashashwini Reddy | Oct 10, 2024
Unveiling the Role of the Analytical Quality Assurance (AQA) Department in Pharma In the world of pharmaceuticals, quality is everything. That’s where the Analytical Quality Assurance (AQA) department steps in, ensuring that every drug produced meets strict...
