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" Generic drug product development : "
edited by Isadore Kanfer, Leon Shargel
Document Type
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BL
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Record Number
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638129
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Doc. No
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dltt
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Title & Author
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Generic drug product development : : international regulatory requirements for bioequivalence /\ edited by Isadore Kanfer, Leon Shargel
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Publication Statement
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New York :: Informa Healthcare,, c2010
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Series Statement
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Drugs and the pharmaceutical sciences ;; 201
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Page. NO
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xxi, 309 p. :: ill. ;; 24 cm
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ISBN
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0849377854 (hardcover : alk. paper)
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: 9780849377853 (hardcover : alk. paper)
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Bibliographies/Indexes
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Includes bibliographical references and index
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Contents
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Australasia / C.T. Hung ... [et al.] -- Brazil / Margareth R.C. Marques, Sílvia Storpirtis, and Márcia Martini Bueno -- Canada / Iain J. McGilveray -- The European Union / Roger K. Verbeeck and Joelle Warlin -- India / Subhash C. Mandal and S. Ravisankar -- Japan / Juichi Riku -- South Africa / Isadore Kanfer, Roderick B. Walker, and Michael F. Skinner -- South America and Pan American Health Organization / Silvia Susana Giarcovich and Ricardo Bolaños -- Taiwan / Li-Heng Pao, Jo-Feng Chi, and Oliver Yoa-Pu Hu -- Turkey / Ilker Kanzik and A. Atilla Hincal -- United States of America / Barbara M. Davit and Dale P. Connor -- The World Health Organization / John Gordon ... [et al.]
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Subject
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Generic drugs
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Subject
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Generic drugs-- Law and legislation
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Subject
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Drugs, Generic-- pharmacokinetics
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Subject
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Drugs, Generic-- standards
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Subject
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Biological Availability
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Subject
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Drug Design
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Subject
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International Cooperation
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Subject
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Legislation, Drug
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Subject
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Therapeutic Equivalency
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Dewey Classification
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615/.19
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LC Classification
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RS55.2.G454 2010
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NLM classification
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W1DR893B v.201 2010
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QV 38G3255 2010
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Added Entry
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Kanfer, Isadore
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Shargel, Leon,1941-
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