by Naveen kumar | 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...
by Naveen kumar | 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 Naveen kumar | 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...
by Naveen kumar | Oct 10, 2024
Disintegration Test for Delayed-Release Tablets and Capsules: A Step-by-Step Guide Are you curious about how delayed-release tablets and capsules are tested to ensure they dissolve at the right time? In the world of pharmaceuticals, it’s crucial that these...
by Naveen kumar | Sep 9, 2024
Calibration vs Validation in the Pharmaceutical Industry In the pharmaceutical world, both calibration and validation are critical processes to ensure accuracy, safety, and compliance with regulatory standards. While these terms are often used together, they serve...