Author(s) :

Dr. S. G. Vaishnav, Dr. G. A. Vaishnav.

Volume/Issue :

Abstract :

A review of manufacturing defects in pharmaceutical tablet dosage form was conducted to provide insight into the causes and prevention of these defects. Poor raw material quality, incorrect process parameters, inadequate cleaning/sanitation, and operator error are amongst the most common factors leading to defects. To reduce the risk of defective tablets, manufacturers should ensure that their raw materials meet quality standards, their processes are correctly controlled, operators receive proper training, sanitation is adequately monitored, and an effective quality management system is implemented. With these measures in place, manufacturers can help improve product quality while ensuring public safety.

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