LEADER 00000cam  2200673Ia 4500 
001    288945451 
003    OCoLC 
005    20200921045832.2 
006    m     o  d         
007    cr cnu---unuuu 
008    081218s2009    flua    ob    001 0 eng d 
020    9781420011678 
020    1420011677 
035    Taylor & Francis All eBooks 
035    (OCoLC)288945451|z(OCoLC)646763344|z(OCoLC)666940961
       |z(OCoLC)779916356|z(OCoLC)1066588839 
035    skip4alma 
037    TANDF_186378|bIngram Content Group 
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049    txum 
050  4 RM301.6|b.C46 2009eb 
072  7 MED|x071000|2bisacsh 
082 04 615/.7|222 
100 1  Chow, Shein-Chung,|d1955- 
245 10 Design and analysis of bioavailability and bioequivalence 
       studies /|cShein-Chung Chow, Jen-pei Liu. 
250    3rd ed. 
260    Boca Raton :|bCRC Press,|c©2009. 
300    1 online resource (xxii, 733 pages) :|billustrations. 
336    text|btxt|2rdacontent 
337    computer|bc|2rdamedia 
338    online resource|bcr|2rdacarrier 
490 1  Chapman & Hall/CRC biostatistics series ;|v27 
504    Includes bibliographical references (pages 647-667) and 
       index. 
505 0  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. 
506    Available only to authorized UTEP users. 
588 0  Print version record. 
650  0 Bioavailability|xResearch|xStatistical methods. 
650  0 Drugs|xTherapeutic equivalency|xResearch|xStatistical 
       methods. 
650 12 Biological Availability. 
650 22 Statistics as Topic|xmethods. 
650 22 Therapeutic Equivalency. 
655  0 Electronic book. 
700 1  Liu, Jen-pei,|d1952- 
776 08 |iPrint version:|aChow, Shein-Chung, 1955-|tDesign and 
       analysis of bioavailability and bioequivalence studies.
       |b3rd ed.|dBoca Raton : CRC Press, ©2009|z9781584886686
       |z1584886684|w(DLC)  2008025461|w(OCoLC)166358489 
830  0 Chapman & Hall/CRC biostatistics series ;|v27. 
856 40 |uhttp://0-www.taylorfrancis.com.lib.utep.edu/books/
       9780429140365|zTo access this resource 
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