9780470887653 - Design and Analysis of Clinical Trials: Concepts and Methodologies di Chow, Shein-Chung; Liu, Jen-Pei (19 risultati)

HRD. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

Condizione: New.

Condizione: New.

Condizione: new.

Condizione: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In good all round condition. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,1750grams, ISBN:9780470887653.

Condizione: Good. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. In good all round condition. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,1750grams, ISBN:9780470887653.

Condizione: New. pp. 928.

Condizione: New. Clinical trials are conducted to allow safety and efficacy data to be collected for health interventions. These trials can only take place once satisfactory information has been gathered on the quality of the non-clinical safety. Series: Wiley Series in Probability and Statistics. Num Pages: 892 pages, charts. BIC Classification: MBGR1; MBNS. Category: (P) Professional & Vocational. Dimension: 255 x 186 x 45. Weight in Grams: 1700. . 2013. 3rd Edition. Hardcover. . . . .

Condizione: New. pp. 928 3rd Edition.

Gebunden. Condizione: New. In summary, this third edition is an impressive expansion beyond a remarkable second edition. This book would be good reference for biostatisticians, clinical researchers, and pharmaceutical scientists in clinical research and development. (Journal of Bio.

Condizione: New. Clinical trials are conducted to allow safety and efficacy data to be collected for health interventions. These trials can only take place once satisfactory information has been gathered on the quality of the non-clinical safety. Series: Wiley Series in Probability and Statistics. Num Pages: 892 pages, charts. BIC Classification: MBGR1; MBNS. Category: (P) Professional & Vocational. Dimension: 255 x 186 x 45. Weight in Grams: 1700. . 2013. 3rd Edition. Hardcover. . . . . Books ship from the US and Ireland.

Hardcover. Condizione: Brand New. 3rd edition. 800 pages. 10.25x7.25x2.00 inches. In Stock.

Condizione: New. pp. 928.

Buch. Condizione: Neu. Neuware - Praise for the Second Edition:'.a grand feast for biostatisticians. It stands ready to satisfy the appetite of any pharmaceutical scientist with a respectable statistical appetite.' --Journal of Clinical Research Best PracticesThe Third Edition of Design and Analysis of Clinical Trials provides complete, comprehensive, and expanded coverage of recent health treatments and interventions. Featuring a unified presentation, the book provides a well-balanced summary of current regulatory requirements and recently developed statistical methods as well as an overview of the various designs and analyses that are utilized at different stages of clinical research and development. Additional features of this Third Edition include:\* New chapters on biomarker development and target clinical trials, adaptive design, trials for evaluating diagnostic devices, statistical methods for translational medicine, and traditional Chinese medicine\* A balanced overview of current and emerging clinical issues as well as newly developed statistical methodologies\* Practical examples of clinical trials that demonstrate everyday applicability, with illustrations and examples to explain key concepts\* New sections on bridging studies and global trials, QT studies, multinational trials, comparative effectiveness trials, and the analysis of QT/QTc prolongation\* A complete and balanced presentation of clinical and scientific issues, statistical concepts, and methodologies for bridging clinical and statistical disciplines\* An update of each chapter that reflects changes in regulatory requirements for the drug review and approval process and recent developments in statistical design and methodology for clinical research and developmentDesign and Analysis of Clinical Trials, Third Edition continues to be an ideal clinical research reference for academic, pharmaceutical, medical, and regulatory scientists/researchers, statisticians, and graduate-level students.

Condizione: As New. Unread book in perfect condition.

Hardcover. Condizione: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Condizione: As New. Unread book in perfect condition.

Hardcover. Condizione: Brand New. 3rd edition. 800 pages. 10.25x7.25x2.00 inches. In Stock. This item is printed on demand.

Hardcover. Condizione: new. Hardcover. Praise for the Second Edition: .a grand feast for biostatisticians. It stands ready to satisfy the appetite of any pharmaceutical scientist with a respectable statistical appetite. Journal of Clinical Research Best Practices The Third Edition of Design and Analysis of Clinical Trials provides complete, comprehensive, and expanded coverage of recent health treatments and interventions. Featuring a unified presentation, the book provides a well-balanced summary of current regulatory requirements and recently developed statistical methods as well as an overview of the various designs and analyses that are utilized at different stages of clinical research and development. Additional features of this Third Edition include: New chapters on biomarker development and target clinical trials, adaptive design, trials for evaluating diagnostic devices, statistical methods for translational medicine, and traditional Chinese medicine A balanced overview of current and emerging clinical issues as well as newly developed statistical methodologies Practical examples of clinical trials that demonstrate everyday applicability, with illustrations and examples to explain key concepts New sections on bridging studies and global trials, QT studies, multinational trials, comparative effectiveness trials, and the analysis of QT/QTc prolongation A complete and balanced presentation of clinical and scientific issues, statistical concepts, and methodologies for bridging clinical and statistical disciplines An update of each chapter that reflects changes in regulatory requirements for the drug review and approval process and recent developments in statistical design and methodology for clinical research and development Design and Analysis of Clinical Trials, Third Edition continues to be an ideal clinical research reference for academic, pharmaceutical, medical, and regulatory scientists/researchers, statisticians, and graduate-level students. Clinical trials are conducted to allow safety and efficacy data to be collected for health interventions. These trials can only take place once satisfactory information has been gathered on the quality of the non-clinical safety. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.