Pharmaceutical Statistics Using SAS (e-bog) af D'Agostino, Ralph
D'Agostino, Ralph (forfatter)

Pharmaceutical Statistics Using SAS e-bog

473,39 DKK (inkl. moms 591,74 DKK)
Pharmaceutical Statistics Using SAS: A Practical Guide offers extensive coverage of cutting-edge biostatistical methodology used in drug development and the practical problems facing today's drug developers. Written by well-known experts in the pharmaceutical industry Alex Dmitrienko, Christy Chuang-Stein, and Ralph D'Agostino, it provides relevant tutorial material and SAS examples to help rea...
E-bog 473,39 DKK
Forfattere D'Agostino, Ralph (forfatter)
Forlag SAS Institute
Udgivet 14 oktober 2015
Længde 460 sider
Genrer Mathematics
Sprog English
Format pdf
Beskyttelse LCP
ISBN 9781629590301
Pharmaceutical Statistics Using SAS: A Practical Guide offers extensive coverage of cutting-edge biostatistical methodology used in drug development and the practical problems facing today's drug developers. Written by well-known experts in the pharmaceutical industry Alex Dmitrienko, Christy Chuang-Stein, and Ralph D'Agostino, it provides relevant tutorial material and SAS examples to help readers new to a certain area of drug development quickly understand and learn popular data analysis methods and apply them to real-life problems. Step-by-step, the book introduces a wide range of data analysis problems encountered in drug development and illustrates them using a wealth of case studies from actual pre-clinical experiments and clinical studies. The book also provides SAS code for solving the problems. Among the topics addressed are these: drug discovery experiments to identify promising chemical compounds animal studies to assess the toxicological profile of these compounds clinical pharmacology studies to examine the properties of new drugs in healthy human subjects Phase II and Phase III clinical trials to establish therapeutic benefits of experimental drugs. Additional features include a discussion of methodological issues, practical advice from subject-matter experts, and review of relevant regulatory guidelines. Most chapters are self-contained and include a fair amount of high-level introductory material to make them accessible to a broad audience of pharmaceutical scientists. This book will also serve as a useful reference for regulatory scientists as well as academic researchers and graduate students. This book is part of the SAS Press program.