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Design and analysis of bioavailabili...
~
Chow, Shein-Chung, (1955-)
Design and analysis of bioavailability and bioequivalence studies /
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Design and analysis of bioavailability and bioequivalence studies /Shein-Chun Chow, Jen-pei Liu.
作者:
Chow, Shein-Chung,
其他作者:
Liu, Jen-pei,
出版者:
Boca Raton :CRC Press,c2009.
面頁冊數:
xxii, 733 p. :ill. ;25 cm.
附註:
"A Chapman & Hall book."
叢書名:
Chapman & Hall/CRC biostatistics series ;
標題:
BioavailabilityResearch
電子資源:
http://www.loc.gov/catdir/toc/ecip0821/2008025461.html
ISBN:
1584886684 (hardback : alk. paper) :
Design and analysis of bioavailability and bioequivalence studies /
Chow, Shein-Chung,1955-
Design and analysis of bioavailability and bioequivalence studies /
Shein-Chun Chow, Jen-pei Liu. - 3rd ed. - Boca Raton :CRC Press,c2009. - xxii, 733 p. :ill. ;25 cm. - Chapman & Hall/CRC biostatistics series ;27.
"A Chapman & Hall book."
Includes bibliographical references (p. 647-667) and index.
Design of bioavailability studies -- Statistical inferences for effects from a standard 2x2 crossover design -- Statistical methods for average bioequivalence -- Power and sample size determination -- Transformation and analysis of individual subject ratios -- Assessment of inter- and intra-subject variabilities -- Assumptions of outlier detection for average bioequivalence -- Optimal crossover designs for two formulations for average bioequivalence -- Assessment of bioequivalence for more than two formulations -- Population and individual bioequivalence -- Statistical procedures for assessment of population and individual bioequivalence -- Assessment of bioequivalence for drugs with negligible plasma levels -- In vitro bioequivalence testing -- In vitro dissolution profiles comparison -- Meta-analysis for bioequivalence review -- Population pharmacokinetics -- Other pharmacokinetic studies -- Review of regulatory guidances on bioequivalence -- Frequently asked questions and future challenges.
ISBN: 1584886684 (hardback : alk. paper) :NT$2968
LCCN: 2008025461
Nat. Bib. Agency Control No.: 101475977DNLMSubjects--Topical Terms:
377593
Bioavailability
--Research
LC Class. No.: RM301.6 / .C46 2009
Dewey Class. No.: 615/.7
National Library of Medicine Call No.: QV 38 / C552d 2009
Design and analysis of bioavailability and bioequivalence studies /
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Design and analysis of bioavailability and bioequivalence studies /
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Design of bioavailability studies -- Statistical inferences for effects from a standard 2x2 crossover design -- Statistical methods for average bioequivalence -- Power and sample size determination -- Transformation and analysis of individual subject ratios -- Assessment of inter- and intra-subject variabilities -- Assumptions of outlier detection for average bioequivalence -- Optimal crossover designs for two formulations for average bioequivalence -- Assessment of bioequivalence for more than two formulations -- Population and individual bioequivalence -- Statistical procedures for assessment of population and individual bioequivalence -- Assessment of bioequivalence for drugs with negligible plasma levels -- In vitro bioequivalence testing -- In vitro dissolution profiles comparison -- Meta-analysis for bioequivalence review -- Population pharmacokinetics -- Other pharmacokinetic studies -- Review of regulatory guidances on bioequivalence -- Frequently asked questions and future challenges.
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http://www.loc.gov/catdir/toc/ecip0821/2008025461.html
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