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Romit Jain, Prashant Vinode*
Sagar Institute of Pharmaceutical Sciences, Sagar (M.P) 470228 India
*Address for Corresponding Author
Prashant Vinode
Sagar Institute of Pharmaceutical Sciences, Sagar (M.P) 470228 India
Abstract
The drug analysis is playing a vital position within the improvement of medicine, their manufacture and therapeutic use for the simultaneous estimation of medicine present in dosage forms, lot of suitable techniques are adopted like UV spectrophotometer HPLC. Those techniques are powerful rugged technique. They are additionally extraordinarily specific, specific, correct, linear and speedy. A pharmaceutical industry depends upon quantitative chemical analysis to make sure that the raw material used and the final product obtained meets the required specification. The drugs may occur as an unmarried factor or multi-issue dosage paperwork. The later proves to be effective because of its mixed mode of movement at the body. This review consists of role of different techniques in the validation of methods for quantitative determinations of drug products.
Keywords: Validation, RP-HPLC method, UV spectrophotometer, quantitative
