Applied Statistics in the Pharmaceutical Industry
With Case Studies Using S-Plus
(Sprache: Englisch)
The purpose of this book is to provide a general guide to statistical methods used in the pharmaceutical industry, and to illustrate how to use S-PLUS to implement these methods. Specifically, the goal is to: Illustrate statistical applications in the...
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Klappentext zu „Applied Statistics in the Pharmaceutical Industry “
The purpose of this book is to provide a general guide to statistical methods used in the pharmaceutical industry, and to illustrate how to use S-PLUS to implement these methods. Specifically, the goal is to: Illustrate statistical applications in the pharmaceutical industry; Illustrate how the statistical applications can be carried out using S-PLUS; Illustrate why S-PLUS is a useful software package for carrying out these applications; Discuss the results and implications of a particular application; The target audience for this book is very broad, including: Graduate students in biostatistics; Statisticians who are involved in the industry as research scientists, regulators, academics, and/or consultants who want to know more about how to use S-PLUS and learn about other sub-fields within the indsutry that they may not be familiar with; Statisticians in other fields who want toknow more about statistical applications in the pharmaceutical industry.
Inhaltsverzeichnis zu „Applied Statistics in the Pharmaceutical Industry “
Statistics and the Drug Development Process, Bruce Rodda and Steven P. Millard One-Factor Comparative Studies, Bill Pikounis Analysis of Animal Carcinogenicity Data, Hongshik Ahn and Ralph L. Kodell Analysis of Toxicokinetic and Pharmacokinetic Data from Animal Studies, Wherly P. Hoffman, Michael A. Heathman, James Z. Chou, and Darrel L. Allen Analysis of Pharmacokinetic Data, Ha Nguyen and Dhammika Amaratunga Graphical Presentation of Single Patient Results, Jürgen Bock Graphical Insight and Data Analysis for the 2, 2, 2, Crossover Design, Bill Pikounis, Tom Bradstreet, and Steven P. Millard Design and Analysis of Phase I Trials in Clinical Oncology, Axel Benner, Lutz Elder, and Gernot Hartung Patient Compliance and its Impact on Steady State Pharmacokinetics, Wenping Wang Analysis of Analgesic Trials, Ene I. Ette, Peter Lockwood, Raymond Miller, and Jaap Mandema Power and Sample Size Calculations, Jürgen Bock Comparing Two Treatments in a Large Phase III Clinical Trial, Michaela Jahn Analysis of Variance: A Comparison Between SAS and S-PLUS, Melvin Olson Permutation Tests for Phase III Clinical Trials, Vance Berger and Anastasia Ivanova Sample Size Reestimation, Wenping Wong and Andreas Krause Meta-Analysis of Clinical Trials, Keith O'Rourke, Beverley Shea, and George A. Wells Analysis of Health Economic Data, John R. Cook, George W. Carides, and Erik J. Dasbach Evaluation of the Decimal Reduction Time of a Sterilization Process in Parmaceutical Production, Jeffrey Eisele, Mauro Gasparini, and Amy Racine Acceptance Sampling Plans by Attributes, Harry Yang and David Carlin
Bibliographische Angaben
- 2001, 2001, 514 Seiten, Maße: 16 x 24,1 cm, Gebunden, Englisch
- Herausgegeben:Millard, Steven P.; Krause, Andreas
- Herausgegeben: Andreas Krause, Steven P. Millard
- Verlag: Springer, New York
- ISBN-10: 0387988149
- ISBN-13: 9780387988146
- Erscheinungsdatum: 27.06.2001
Sprache:
Englisch
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