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 | Sep 6, 2024
SOP For Operation of friability apparatus 1.0 OBJECTIVE To define the procedure for the operation and calibration of the friability test apparatus used in tablet testing. 2.0 SCOPE This Standard Operating Procedure (SOP) applies to the Production department. 3.0...
by Naveen kumar | Jul 14, 2024
Importance of Tablet Disintegration and Disintegration Times of Different Types of Tablets Disintegration is an important step for a tablet formulation as it allows the tablet to break down into smaller particles within an appropriate time frame after...
by Naveen kumar | Jun 2, 2024
Guidelines for Tablet Friability Determination as per United States Pharmacopeia Why Friability test is Performed – In this article we are going into detail about the friability test, how it is performed as per guidelines, the number of samples to be taken for...
by Naveen kumar | May 15, 2024
The disintegration test is a quality control test performed to check whether the dosage forms like tablets, capsules, and suppositories disintegrate within the expected time when these dosage forms are kept in the required medium. This test is done to ensure no...
