A REVIEW ON COMPARATIVE STUDY OF IN-PROCESS AND FINISHED PRODUCTS QUALITY CONTROL TESTS FOR STERILE AND NON STERILE DOSAGE FORM

In a pharmaceutical organization a quality control is a fundamental segment that refers to a process of striving to produce a product by a series of in process quality control test in order to eliminate or prevent error at any stage of production. The study deals with in process product quality control tests for sterile and non sterile dosage forms taking compendia specifications of IP, BP, USP. Those all quality control test which carried out during the manufacturing of product or before marketing of the product denote as in process quality control test . In process Quality control deals with testing, sampling, specification, documentation which ensure that all tests are actually carried out prior to release of material for sale or use. This is the most ideal approach for determining the pharmaceutical quality of the finished dosage form. This article deals with quality control of sterile dosage form (parenteral and ophthalmic) and non sterile dosage form (tablets, capsules etc.). Pharmaceutical Sciences