Table of contents for Handbook of isolation and characterization of impurities in pharmaceuticals / edited by Satinder Ahuja, Karen Mills Alsante.
Bibliographic record and links to related information available from the Library of Congress catalog
Information from electronic data provided by the publisher. May be incomplete or contain other coding.
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