by Dr. Yashashwini Reddy | Aug 8, 2025
Investigation of OOS Results in Analytical Testing 1. What is an OOS Result? An Out-of-Specification (OOS) result is any analytical test result that falls outside the established acceptance criteria/specifications outlined in an approved method, regulatory filing, or...
by Dr. Yashashwini Reddy | May 6, 2025
The Instrument and Equipment List for Pharmaceuticals refers to the various tools, devices, and machinery used in the pharmaceutical industry to conduct research, development, production, and quality control. These instruments ensure the safe, efficient, and compliant...
by Dr. Yashashwini Reddy | May 3, 2025
Tablet Manufacturing Process: An Overview The tablet manufacturing process is a complex and precise procedure that transforms raw materials into the final pharmaceutical or nutraceutical product. The process involves several key stages, each critical to ensuring the...
by Dr. Yashashwini Reddy | May 1, 2025
“Ensuring Accuracy in Pharmaceutical UV Cabinet Calibration” refers to the critical process of calibrating ultraviolet (UV) cabinets used in pharmaceutical manufacturing and laboratory environments to ensure they provide accurate, reliable, and consistent...
by Dr. Yashashwini Reddy | May 1, 2025
Methodology for Calibrating a Tablet Friability Tester The friability test is crucial in the pharmaceutical industry for assessing the durability and mechanical strength of tablets. A friability tester is used to evaluate how well tablets withstand mechanical stress...
