MPG.eBooks - Table of Contents: Pharmaceutical statistics using SAS

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Bibliographic Details
Main Author:	Dmitrienko, Alex
Other Authors:	Chuang-Stein, Christy, D'Agostino, Ralph B.
Format:	eBook
Language:	English
Published:	Cary, N.C. SAS Institute 2007
Series:	SAS Press series
Subjects:	Pharmacology / Aat Medical / Nursing / Pharmacology / Bisacsh Medical / Pharmacology / Bisacsh Drugs / Testing / Statistical Methods Drugs / Testing / Statistical Methods / Fast Drugs / Testing / Statistical Methods / Blmlsh Pharmacology / Http://id.loc.gov/authorities/subjects/sh85100599 Medical / Pharmacy / Bisacsh Pharmacologie Drug Development / Fast Sas (computer File) / Http://id.loc.gov/authorities/names/n88028236 Drug Development / Blmlsh Pharmacology / Blmlsh Clinical Trials As Topic Information Storage And Retrieval Sas (computer File) / Fast Clinical Pharmacology / Blmlsh Clinical Trials / Fast Pharmacology, Clinical Médicaments / Développement Clinical Pharmacology / Http://id.loc.gov/authorities/subjects/sh90000174 Pharmacology Data Interpretation, Statistical Clinical Trials / Http://id.loc.gov/authorities/subjects/sh85027069 Pharmacologie Clinique Sas (computer File) / Blmlsh Pharmacology / Fast Clinical Trials / Blmlsh Clinical Pharmacology / Fast Études Cliniques Drug Development / Http://id.loc.gov/authorities/subjects/sh97007921 Médicaments / Essais Cliniques / Méthodes Statistiques Medical / Drug Guides / Bisacsh
Online Access:	https://learning.oreilly.com/library/view/~/978159...
Collection:	O'Reilly - Collection details see MPG.ReNa

Table of Contents:

Includes bibliographical references and index
Statistics in drug development by Christy Chuang-Stein and Ralph D'Agostino
Modern classification methods for drug discovery by Kjell Johnson and William Rayens
Model building techniques in drug discovery by Kimberly Crimin and Thomas Vidmar
Statistical considerations in analytical method validation by Bruno Boulanger, Viswanath Devanaryan, Walthère Dewé, and Wendell Smith
Some statistical considerations in nonclinical safety assessment by Wherly Hoffman, Cindy Lee, Alan Chiang, Kevin Guo, and Daniel Ness
Nonparametric methods in pharmaceutical statistics by Paul Juneau
Optimal design of experiments in pharmaceutical applications by Valerii Fedorov, Robert Gagnon, Sergei Leonov, and Yuehui Wu
Analysis of human pharmacokinetic data by Scott Patterson and Brian Smith
Allocation in randomized clinical trials by Olga Kuznetsova and Anastasia Ivanova
Sample-size analysis for traditional hypothesis testing: concepts and issues by Ralph G. O'Brien and John Castelloe
Design and analysis of dose-ranging clinical studies by Alex Dmitrienko, Kathleen Fritsch, Janson Hsu, and Stephen Ruberg
Analysis of incomplete data by Geert Molenberghs, Caroline Beunckens, Herbert Thijs, Ivy Jansen, Geert Verbeke, Michael Kenward, and Kristen Van Steen
Reliability and validity: Assessing the psychometric properties of rating scales by Douglas Faries and Ilker Yalcin
Decision analysis in drug development by Carl-Fredrik Burman, Andy Grieve, and Stephen Senn