World Journal of
Pharmaceutical and Life Sciences

( An ISO 9001:2015 Certified International Journal )

An International Peer Reviewed Journal for Pharmaceutical and Life Sciences
An Official Publication of Society for Advance Healthcare Research (Reg. No. : 01/01/01/31674/16)
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Abstract

TO STUDY THE QUALITY CONTROL PARAMETERS FOR UNCOATED PARACETAMOL & NIMESULIDE TABLET IN PHARMACEUTICAL INDUSTRY

*Viralbhai A. Prajapati, Mona A. Gupta, Prof. Dr. C. N. Patel, Prof. Dr. Pankaj H. Prajapati, Dr. Hitesh D. Karen, Dr. Laxman M. Prajapati and Prof. Dr. Dhrubo Jyoti Sen

ABSTRACT

A pharmaceutical uncoated tablet must satisfy certain standards to claim it to be a quality drug. The quality of any drug in dosage form is its safety, potency, stability, patient acceptability and compliance. The quality of tablet needs to be designed from the product development stage. Quality control test for uncoated tablet is strongly related to final product quality because checks performed during production in order to monitor and if necessary, to adjust the process to ensure that the product conform to its specification are the key for the good or excellence quality of a tablet. The main purpose of quality control test for uncoated tablet is to produce a perfect finished product quality control (FPQC) test for tablet are performed with specific quality control test or parameters within acceptance limit or not. The aim of this to study in process quality control test carried for uncoated Paracetamol & Nimesulide.

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