by Dr. Yashashwini Reddy | Aug 9, 2025
GMP Requirements in Pharmaceuticals Good Manufacturing Practice (GMP) is a regulatory framework ensuring that pharmaceutical products are consistently produced and controlled according to quality standards, minimizing risks to patients. 1. Quality Management System...
by Dr. Yashashwini Reddy | Jun 9, 2025
Sampling in Cleaning Validation in Pharmaceutical Industry Cleaning Validation is a crucial part of pharmaceutical manufacturing to ensure that equipment and production areas are properly cleaned to prevent cross-contamination, ensure product quality, and comply with...
by Dr. Yashashwini Reddy | May 13, 2025
Standard Operating Procedure (SOP) Here’s a Standard Operating Procedure (SOP) for the Cleaning of a Vibro Sifter, typically used in pharmaceutical, food, or chemical manufacturing. You should tailor it to your specific equipment, cleaning agents, and...
by Dr. Yashashwini Reddy | Apr 29, 2025
Non-conformance in the pharmaceutical industry refers to deviations from established standards, regulations, or specifications in the production, packaging, labeling, or testing of pharmaceutical products. These deviations can lead to serious consequences, including...
by Dr. Yashashwini Reddy | Apr 23, 2025
Standard Operating Procedure (SOP) Here is a Standard Operating Procedure (SOP) for the Operation and Calibration of Friability Test Apparatus. This SOP ensures proper operation, calibration, and maintenance of the friability testing...
