Analytical methods are critical in quality assurance for the pharmaceutical industry. Keeping this in mind the author made an attempt to establish novel analytical techniques for some of the most significant pharmaceuticals in both pure and prescription dose forms. There are no complicated or time-consuming procedures detailed in this thesis. In addition to internal control the technology might be utilized for process development of bulk pharmaceuticals as well. In all five chapters were dedicated to the investigation's work.In my present investigation - simple precise and accurate HPLC UPLC andLC-MS/MS methods have been developed and validated for the analysis ofselected drugs.
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