by Dr. Yashashwini Reddy | Apr 29, 2025
The essential GMP (Good Manufacturing Practice) compliance requirements for pharmaceuticals are designed to ensure the consistent production of high-quality, safe, and effective medicinal products. These requirements are globally recognized and enforced by regulatory...
by Dr. Yashashwini Reddy | Apr 19, 2025
1. What is OOS in the pharmaceutical industry? OOS stands for “Out of Specification.” It refers to test results that fall outside the predefined acceptance criteria set by regulatory authorities or internal specifications. Interviewers want to ensure you...
by Dr. Yashashwini Reddy | Nov 28, 2024
Basic Guidelines for Process Validation in Tablet Manufacturing Process validation is a critical component of pharmaceutical manufacturing that ensures each batch of tablets meets quality, safety, and efficacy standards. The following guidelines outline the...
by Dr. Yashashwini Reddy | Nov 26, 2024
1. What are pharmaceutical pellets? Pellets are small, spherical, or semi-spherical solid dosage forms used in pharmaceutical formulations to ensure controlled drug release, improve bioavailability, and facilitate drug delivery. 2. What are the advantages of...
by Dr. Yashashwini Reddy | Nov 25, 2024
Terminal Sterilization Methods in Pharmaceuticals Terminal sterilization is a key process in pharmaceutical manufacturing to ensure that drug products are free of harmful microorganisms. It is performed on the final product, typically in its sealed container, to...
