Author(s): V. Shirisha, Somsubhra Ghosh, B. Rajni, David Banji

Email(s): som_subhra_ghosh@yahoo.co.in

DOI: Not Available

Address: V. Shirisha, Somsubhra Ghosh*, B. Rajni, David Banji
Department of Pharmaceutical Analysis and Quality Assurance, Nalanda College of Pharmacy, Cherlapally, Nalgonda, 508001, A. P, India.
*Corresponding Author

Published In:   Volume - 7,      Issue - 2,     Year - 2014


ABSTRACT:
Present study deals with a brief overview of comparative study of quality requirements for in process and finished product quality control test of IP, BP and USP for some conventional dosage forms. The concept of IPQC refers to the process of striving to produce a quality product by a series of measures requiring an organised effort in order to eliminate errors at every stage in the production. Main function of IPQC is monitoring and if necessary adaption of the manufacturing process in order to comply with the specifications this may include control of equipment and environment. In process materials should be tested for identity, strength and quality and purity as appropriate and approved (or) rejected by the quality Assurance department. During the production process rejected in process materials should be identified and controlled under a Quarantine system designed to prevent their use in manufacturing. IPQC is done to comply Concurrent Validation also.


Cite this article:
V. Shirisha, Somsubhra Ghosh, B. Rajni, David Banji. An Updated Review on IPQC Tests for Sterile and Non Sterile Products. Research J. Pharm. and Tech. 7(2): Feb. 2014; Page 255-265.


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