by Naveen kumar | Nov 27, 2024
Q1. What is disintegration, and why is it important in tablet evaluation? A: Disintegration is the process by which a tablet breaks down into smaller fragments in a liquid medium to release its active ingredients. It is important because proper disintegration is a...
by Naveen kumar | Nov 27, 2024
Q1. What are the flow properties of powders, and why are they important in the pharmaceutical industry? A: Flow properties refer to the ability of a powder to move or flow under specified conditions. They are critical in pharmaceutical processes such as tablet...
by Naveen kumar | Nov 27, 2024
Q1. Why is microbiology important in the pharmaceutical industry? A: Microbiology ensures that pharmaceutical products are free from microbial contamination. It plays a crucial role in sterility testing, microbial limit testing, and environmental monitoring to...
by Naveen kumar | Nov 27, 2024
1. What is Developmental Quality Assurance (DQA)? A: Developmental Quality Assurance ensures that quality is built into a product during its development stages. It involves reviewing documents, processes, and protocols to meet regulatory and quality standards...
by Naveen kumar | Nov 27, 2024
Interview Questions and Answers for Drug Substance (3.2.S) in CTD – Regulatory Affairs (Freshers) 1. What is the role of 3.2.S in the CTD (Common Technical Document)? Answer: The 3.2.S section of the CTD is dedicated to the “Drug Substance,” which...
