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 26, 2024
“Top 20 Interview Questions on Semi-Solid Dosage Forms for Pharma Freshers” 1. What are semi-solid dosage forms? These are pharmaceutical preparations with a consistency between solid and liquid, designed for topical, transdermal, or rectal application...
by Naveen kumar | Nov 26, 2024
1. What is tablet coating? Tablet coating is the process of applying a thin layer of coating material to a tablet’s surface to protect it, improve its appearance, or modify its drug release profile. 2. What are the main types of tablet coatings? Sugar coating –...
by Naveen kumar | Nov 1, 2024
Understanding the Difference Between Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs) in Pharmaceuticals In pharmaceutical manufacturing, maintaining high product quality is essential, and two important concepts—Critical Quality Attributes...
by Naveen kumar | Oct 13, 2024
Understanding Dwell Time in Tablet Compression In pharmaceutical manufacturing, the quality and integrity of tablets are paramount. One critical aspect that significantly influences these factors is dwell time. This article will explore what dwell time is, its...
