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Biostatistics in Biopharmaceutical Research and Development: Clinical Trial Analysis, Volume 2 2024 ed. [Hardback]

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  • Formāts: Hardback, 517 pages, height x width: 235x155 mm, 168 Illustrations, black and white; XVIII, 517 p. 168 illus., 1 Hardback
  • Izdošanas datums: 26-Dec-2024
  • Izdevniecība: Springer International Publishing AG
  • ISBN-10: 3031659368
  • ISBN-13: 9783031659362
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  • Formāts: Hardback, 517 pages, height x width: 235x155 mm, 168 Illustrations, black and white; XVIII, 517 p. 168 illus., 1 Hardback
  • Izdošanas datums: 26-Dec-2024
  • Izdevniecība: Springer International Publishing AG
  • ISBN-10: 3031659368
  • ISBN-13: 9783031659362
Citas grāmatas par šo tēmu:
The Deming Conference on Applied Statistics has long been deemed an influential event in the biostatistics and biopharmaceutical profession. It provides learning experience on recent developments in statistical methodologies in biopharmaceutical applications and FDA regulations.





This book honors 80 years of contributions and dedication of the Deming Conference in biostatistics, and biopharmaceutical clinical trial methodology and applications. All chapters are contributed by world-class and prominent Deming speakers, who've contributed their cutting-edge research and developments to the community. Volume 2 covers Biomarkers in Drug Development, Time-To-Event Data Analysis and Methods, and emerging development in biopharmaceutical biostatistics.





This book aims to booster research, education, and training in biostatistics and in biopharmaceutical research and development. 
Statistical Challenges in the Analysis of Biomarker Data.- 2.  
 Evaluating Predictive Accuracy of Prognostic Model for Censored
Time-to-Event Data Analysis in Clinical Trials.- Statistical Methods for
Accommodating Immortal Time: A Selective Review and Comparison.- Variable
selection for partially functional additive Cox Model with interval-censored
failure time data.- A Bayesian proportional hazards model to predict patient
recruitment in multicenter clinical trials.- GET MORE INFORMATION FROM
RECURRENT EVENTS DATA.- Introduction to Patient Preference Studies.- Machine
Learning for Precision Medicine and Humanized AI for Future Healthcare.- The
Statistical Evaluation of Surrogate Endpoints in Clinical
Trials.- Treatment Effect Estimation Using Data from Observational and
Non-Randomized Studies.- Methods for Comparing Two Treatments for a
Dichotomous Outcome for a Two-Period Design with Treatment Switching of
Control Group Period 1 Non-Responders.- Regression-based estimation of
optimal adaptive treatment strategies: Key methods.- Vaccine
Disease-Prevention Efficacy Studies: Traditional Approaches and New
Frontiers.- Covariate Adjustment in Analyzing Randomized Clinical
Trials: Approaches, Software, and Application.- Joint correlated
responses and feedback effect with time-dependent covariates.- Distributions
and Their Approximations for P-Values.
Dr. Ding-Geng  Chen is a Fellow of the American Statistical Association and is currently the executive director and professor in biostatistics at the College of Health Solutions, Arizona State University. He is also an Extraordinary Professor and the SARChI in biostatistics at the University of Pretoria, and an honorary professor at the University of KwaZulu-Natal, South Africa. He is a senior biostatistics consultant for biopharmaceuticals and government agencies with extensive expertise in biostatistics, clinical trials, and public health statistics. Dr. Chen has more than 200 referred professional publications and co-authored 11 books and co-edited 24 books on clinical trial methodology, meta-analysis, data science, causal inference, and public health research. Professor Chen is the Deming publicity chair and he has been honored with the "Award of Recognition" from the Deming Conference Committee for highly successful advanced biostatistics workshop tutorials with his books.