A key component of the overall quality of a pharmaceutical is control of impurities, as their presence, even in small amounts, may affect drug safety and efficacy. The identification and quantification of impurities to acceptable standards presents a significant challenge to the analytical chemist. Analytical science is developing rapidly and provides increasing opportunity to identify the structure, and therefore the origin and safety implications of these impurities, and the challenges of their measurement drives the ...
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A key component of the overall quality of a pharmaceutical is control of impurities, as their presence, even in small amounts, may affect drug safety and efficacy. The identification and quantification of impurities to acceptable standards presents a significant challenge to the analytical chemist. Analytical science is developing rapidly and provides increasing opportunity to identify the structure, and therefore the origin and safety implications of these impurities, and the challenges of their measurement drives the development of modern quantitative methods. Written for both practicing and student analytical chemists, Analysis of Drug Impurities provides a detailed overview of the challenges and the techniques available to permit accurate identification and quantification of drug impurities.
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Add this copy of Analysis of Drug Impurities to cart. $162.38, very good condition, Sold by Sunny Day Books rated 4.0 out of 5 stars, ships from Mayer, AZ, UNITED STATES, published 2007 by Wiley-Blackwell.
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Seller's Description:
Very Good. Owners name stamped on flyleaf and page ends. Former library copy with very discreet markings. Text in clean/unmarked condition. Cover has minor shelf rubbings. Binding is tight.
