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Statistical Issues in Drug Development 3e (Hardcover, 3rd Edition): S Senn Statistical Issues in Drug Development 3e (Hardcover, 3rd Edition)
S Senn
R2,360 Discovery Miles 23 600 Ships in 12 - 17 working days

Statistical Issues in Drug Development The revised third edition of Statistical Issues in Drug Development delivers an insightful treatment of the intersection between statistics and the life sciences. The book offers readers new discussions of crucial topics, including cluster randomization, historical controls, responder analysis, studies in children, post-hoc tests, estimands, publication bias, the replication crisis, and many more. This work presents the major statistical issues in drug development in a way that is accessible and comprehensible to life scientists working in the field, and takes pains not to gloss over significant disagreements in the field of statistics, while encouraging communication between the statistical and life sciences disciplines. In addition to new material on topics like invalid inversion, severity, random effects in network meta-analysis, and explained variation, readers will benefit from the inclusion of: A thorough introduction to basic topics in drug development and statistics, including the role played by statistics in drug development An exploration of the four views of statistics in drug development, including the historical, methodological, technical, and professional An examination of debatable and controversial topics in drug development, including the allocation of treatments to patients in clinical trials, baselines and covariate information, and the measurement of treatment effects Perfect for life scientists and other professionals working in the field of drug development, Statistical Issues in Drug Development is the ideal resource for anyone seeking a one-stop reference to enhance their understanding of the use of statistics during drug development.

Cross-over Trials in Clinical Research 2e (Hardcover, 2nd Edition): S Senn Cross-over Trials in Clinical Research 2e (Hardcover, 2nd Edition)
S Senn
R2,986 Discovery Miles 29 860 Ships in 12 - 17 working days

Cross-over trials are an important class of design used in the pharmaceutical industry and medical research, and their use continues to grow. Cross-over Trials in Clinical Research, Second Edition has been fully updated to include the latest methodology used in the design and analysis of cross-over trials. It includes more background material, greater coverage of important statistical techniques, including Bayesian methods, and discussion of analysis using a number of statistical software packages.

  • Comprehensive coverage of the design and analysis of cross-over trials.

  • Each technique is carefully explained and the mathematics is kept to a minimum.

  • Features many real and original examples, taken from the author's vast experience.

  • Includes discussion of analysis using SAS, S-Plus and, GenStat, StatXact and Excel.

  • Written in a style suitable for statisticians and physicians alike.
Primarily aimed at statisticians and researchers working in the pharmaceutical industry, the book will also appeal to physicians involved in clinical research and students of medical statistics.
Statistical Issues in Drug Development (Hardcover, 2nd Edition): Stephen S. Senn Statistical Issues in Drug Development (Hardcover, 2nd Edition)
Stephen S. Senn
R2,865 R2,308 Discovery Miles 23 080 Save R557 (19%) Out of stock

Drug development is the process of finding and producing therapeutically useful pharmaceuticals, turning them into safe and effective medicine, and producing reliable information regarding the appropriate dosage and dosing intervals. With regulatory authorities demanding increasingly higher standards in such developments, statistics has become an intrinsic and critical element in the design and conduct of drug development programmes.

"Statistical Issues in Drug Development" presents an essential and thought provoking guide to the statistical issues and controversies involved in drug development.

This highly readable second edition has been updated to include: Comprehensive coverage of the design and interpretation of clinical trials. Expanded sections on missing data, equivalence, meta-analysis and dose finding. An examination of both Bayesian and frequentist methods. A new chapter on pharmacogenomics and expanded coverage of pharmaco-epidemiology and pharmaco-economics. Coverage of the ICH guidelines, in particular ICH E9, Statistical Principles for Clinical Trials.

It is hoped that the book will stimulate dialogue between statisticians and life scientists working within the pharmaceutical industry. The accessible and wide-ranging coverage make it essential reading for both statisticians and non-statisticians working in the pharmaceutical industry, regulatory bodies and medical research institutes. There is also much to benefit undergraduate and postgraduate students whose courses include a medical statistics component.

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