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A practical guide for chemists in the pharmaceutical industry to making automated analyses of drugs that will meet the standards of regulatory agencies. Reviews the standard techniques of high-performance liquid chromatography, specialized detection methods, automation in pharmaceutical analysis, an

Produktbeschreibung
A practical guide for chemists in the pharmaceutical industry to making automated analyses of drugs that will meet the standards of regulatory agencies. Reviews the standard techniques of high-performance liquid chromatography, specialized detection methods, automation in pharmaceutical analysis, an
Autorenporträt
GODWIN W. FONG is Director of Quality Control Laboratories for the Super pharm Corporation in Bayshore, New York. Previously, he was Assistant Director in Re¬search & Development at SmithKline Beecham Pharmaceuticals, King of Prussia, Pennsylvania. The author or coauthor of many publications and abstracts, Dr. Fong is a member of the American Chemical Society, American Association of Pharma¬ceutical Scientists, and American Association for the Advancement of Science, among others. Dr. Fong received the B.S. degree (1974) in chemistry from the State Uni¬versity of New York at Stony Brook, and Ph.D. degree (1980) in chemistry from the State University of New York at Buffalo. STANLEY K. LAM is Associate Professor of Laboratory Medicine and Director of the Drug Analysis and Special Chemistry Laboratory at the Albert Einstein College of Medicine, Bronx, New York. The author or coauthor of numerous scientific articles, book chapters, and abstracts, as well as editor of one book, Dr. Lam is a member of the American Chemical Society, American Association of Clinical Chemists, and American Association for the Advancement of Science. Dr. Lam received the B.A. degree (1974) in chemistry from California State University, Sacramento, and Ph.D. degree (1980) in chemistry from the State University of New York at Buffalo.