by Naveen kumar | Jul 20, 2024
Recovery Factor in Cleaning Validation: Procedure and Importance In the cleaning validation, the recovery factor plays a crucial role in determining how effectively residues can be removed from equipment surfaces. This metric ensures the precision of analytical...
by Naveen kumar | Jul 20, 2024
Cleaning Validation in Manufacturing: Ensuring Effective Procedures Cleaning validation is done to measure the effectiveness of cleaning procedures in removing residues from previous products. After the execution of a batch, the equipment must be cleaned according to...
by Naveen kumar | Jul 12, 2024
Pharmaceutical interview questions – In this article, we have presented a few pharmaceutical interview questions asked in the Quality assurance interview. These are basic questions related to the friability test and the disintegration test. 1. Number of tablets...
by Naveen kumar | Jul 1, 2024
A product needs to be tested and proven for its quality and compliance requirements before it reaches the factory to the consumer. With the increasing complexity of the equipment being manufactured as per consumer demand, there is a chance for countless errors. So,...
by Naveen kumar | Jun 13, 2024
In this article we are going to learn about BMR – Batch Manufacturing Record 1.A BMR is a written documentation containing information on how a batch will be manufactured. 2. It Contains Step by step instructions on how a batch will be manufactured. 3. BMR is...
