by Dr. Yashashwini Reddy | Apr 20, 2025
Standard Operating Procedure (SOP) Purpose: To outline the procedure for the inspection, sampling, and approval or rejection of incoming raw materials to ensure they meet the required quality standards. Scope: This procedure...
by Dr. Yashashwini Reddy | Apr 19, 2025
1. What are GLP, GDP, and GMP, and how do they differ? This foundational question tests your understanding of the definitions: GLP: Ensures integrity and quality of non-clinical lab studies. GDP: Ensures data integrity and accuracy in documentation. GMP: Ensures...
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 | Apr 17, 2025
1. What is NMR spectroscopy? NMR spectroscopy is an analytical technique used to determine the structure of organic compounds by analyzing the magnetic properties of atomic nuclei. It provides detailed information about the number, types, and environments of atoms in...
by Dr. Yashashwini Reddy | Dec 1, 2024
Classification of GMP Deficiencies: A Comprehensive Guide for Pharmaceutical Compliance Good Manufacturing Practice (GMP) is a cornerstone of pharmaceutical manufacturing, ensuring that products are produced and controlled according to rigorous quality standards....
