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140905s2014 xxu| s |||| 0|eng d |
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|a 9781493912520
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|a 10.1007/978-1-4939-1252-0
|2 doi
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|a Sistema de Bibliotecas del Tecnológico de Costa Rica
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|a FDA Bioequivalence Standards /
|c edited by Lawrence X. Yu, Bing V. Li.
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|a 1st ed. 2014.
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|a New York, NY :
|b Springer New York :
|b Imprint: Springer,
|c 2014.
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|a XIII, 465 p. 58 illus., 26 illus. in color. :
|b online resource.
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a AAPS Advances in the Pharmaceutical Sciences Series,
|v 13
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|a 1 Bioequivalence History -- 2 Fundamentals of Bioequivalence -- 3 Basic Statistical Considerations -- 4 The Effects of Food on Drug Bioavailability and Bioequivalence -- 5 Bio waiver and Biopharmaceutics Classification System -- 6 Bioequivalence of Highly Variable Drugs -- 7 Partial Area under the Curve: An Additional Pharmacokinetic Metric for Bioavailability and Bioequivalence Assessments -- 8 Bioequivalence for Narrow Therapeutic Index Drugs -- 9 Pharmacodynamic Endpoint-based Bioequivalence Studies -- 10 Clinical Endpoint Bioequivalence Study -- 11 Bioequivalence for Liposomal Drug Products -- 12 Bioequivalence for Drug Products Acting Locally within Gastrointestinal Tract -- 13 Bioequivalence for Topical Drug Products -- 14 Bioequivalence for Orally Inhaled and Nasal Drug Products -- 15 Bioequivalence: Modeling and Simulation -- 16 Bioanalysis.
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|a Pharmaceutical technology.
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|a Pharmaceutical Sciences/Technology.
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|a Yu, Lawrence X.
|e editor.
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|a Li, Bing V.
|e editor.
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710 |
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|a SpringerLink (Online service)
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|t Springer eBooks
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