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- 2008025461 contributor B11101469.
- 2008025461 contributor B11101470.
- 2008025461 created "c2009.".
- 2008025461 date "2009".
- 2008025461 date "c2009.".
- 2008025461 dateCopyrighted "c2009.".
- 2008025461 description "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.".
- 2008025461 description "Includes bibliographical references (p. 647-667) and index.".
- 2008025461 extent "xxii, 733 p. :".
- 2008025461 identifier "1584886684 (hardback : alk. paper)".
- 2008025461 identifier "9781584886686 (hardback : alk. paper)".
- 2008025461 identifier 2008025461.html.
- 2008025461 isPartOf "Chapman & Hall/CRC biostatistics series ; 27".
- 2008025461 issued "2009".
- 2008025461 issued "c2009.".
- 2008025461 language "eng".
- 2008025461 publisher "Boca Raton : CRC Press,".
- 2008025461 subject "2008 M-918".
- 2008025461 subject "615/.7 22".
- 2008025461 subject "Bioavailability Research Statistical methods.".
- 2008025461 subject "Biological Availability.".
- 2008025461 subject "Drugs Therapeutic equivalency Research Statistical methods.".
- 2008025461 subject "QV 38 C552d 2009".
- 2008025461 subject "RM301.6 .C46 2009".
- 2008025461 subject "Statistics as Topic methods.".
- 2008025461 subject "Therapeutic Equivalency.".
- 2008025461 tableOfContents "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.".
- 2008025461 title "Design and analysis of bioavailability and bioequivalence studies / Shein-Chun Chow, Jen-pei Liu.".
- 2008025461 type "text".