Table of contents for Handbook of isolation and characterization of impurities in pharmaceuticals / edited by Satinder Ahuja, Karen Mills Alsante.


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Counter OVERVIEW: ISOLATION AND CHARACTERIZATION OF IMPURITIES
REVIEW OF REGULATORY GUIDANCE ON IMPURITIES POLYMORPHIC & SOLVATOMORPHIC IMPURITIES IMPURITIES IN DRUG PRODUCTS STRATEGIES FOR INVESTIGATION AND CONTROL OF PROCESS AND DEGRADATION-RELATED IMPURITIES REFERENCE STANDARDS SAMPLE SELECTION FOR ANALYTICAL METHOD DEVELOPMENT SAMPLE PREPARATION METHODS ISOLATION METHODS I: THIN-LAYER CHROMATOGRAPHY ISOLATION METHODS II: COLUMN CHROMATOGRAPHY MASS SPECTRAL CHARACTERIZATION NMR CHARACTERIZATION OF IMPURITES HYPHENATED CHARACTERIZATION TECHNIQUES SOLVING IMPURITY/DEGRADATION PROBLEMS: CASE STUDIES

Library of Congress subject headings for this publication: Drugs Purification Handbooks, manuals, etc, Drugs Separation Handbooks, manuals, etc, Pharmaceutical Preparations analysis Handbooks, Pharmaceutical Preparations analysis Laboratory Manuals, Drug Contamination prevention & control Handbooks, Drug Contamination prevention & control Laboratory Manuals, Pharmaceutical Preparations standards Handbooks, Pharmaceutical Preparations standards Laboratory Manuals, Technology, Pharmaceutical methods Handbooks, Technology, Pharmaceutical methods Laboratory Manuals