Isbn: 9780470046081 - management of data in clinical trials: 23 (31 risultati)

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Hardback. Condizione: Good. This book explores data management from study development to final analysis and suggests alternative approaches, with guidelines on optimal approaches under various circumstances. It contains discussions of the various approaches to clinical trials for some of the major diseases. This second edition compares approaches in the U.S.…

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Condizione: New. Brand New. Soft Cover International Edition. Different ISBN and Cover Image. Priced lower than the standard editions which is usually intended to make them more affordable for students abroad. The core content of the book is generally the same as the standard edition. The country selling restrictions may be printed on the book but is no problem for the self-use. This Item maybe shipped from US or any other country as we have multiple locations worldwide.…

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Condizione: New. pp. xii + 190 2nd Edition.

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Condizione: New. pp. xii + 190 Illus.

Condizione: New. This book explores data management from study development to final analysis and suggests alternative approaches, with guidelines on optimal approaches under various circumstances. It contains discussions of the various approaches to clinical trials for some of the major diseases. This second edition compares approaches in the U.S. Series: Wiley Series in Probability and Statistics. Num Pages: 208 pages, Illustrations. BIC Classification: MBGR; MBNS. Category: (P) Professional & Vocational. Dimension: 237 x 164 x 17. Weight in Grams: 486. . 2007. 2nd Edition. Hardcover. . . . . …

Condizione: New. Eleanor McFadden is Managing Director at Frontier Science (Scotland) Ltd. in the United Kingdom and is the current president of the Society for Clinical Trials. With almost thirty years of experience in clinical trials data management in both academia and i.

Hardcover. Condizione: Brand New. 2nd edition. 190 pages. 9.25x6.25x0.50 inches. In Stock.

Condizione: New. This book explores data management from study development to final analysis and suggests alternative approaches, with guidelines on optimal approaches under various circumstances. It contains discussions of the various approaches to clinical trials for some of the major diseases. This second edition compares approaches in the U.S. Series: Wiley Series in Probability and Statistics. Num Pages: 208 pages, Illustrations. BIC Classification: MBGR; MBNS. Category: (P) Professional & Vocational. Dimension: 237 x 164 x 17. Weight in Grams: 486. . 2007. 2nd Edition. Hardcover. . . . . Books ship from the US and Ireland. …

Buch. Condizione: Neu. Neuware - A valuable new edition of the trusted, practical guide to managing data in clinical trialsRegardless of size, type, or complexity, accurate results for any clinical trial are ultimately determined by the quality of the collected data. Management of Data in Clinical Trials, Second Edition explores data management and trial organization as the keys to developing an accurate and reliable clinical trial. With a focus on the traditional aspects of data collection as well as recent advances in technology, this new edition provides a complete and accessible guide to the management structure of a clinical trial, from planning and development to design and analysis. Practical approaches that result in the collection of complete and timely data are also provided.While maintaining a comprehensive overview of the knowledge and tools that are essential for the organization of a modern clinical trial, the author has expanded the topical coverage in the Second Edition to reflect the possible uses of recent advances in technology in the data collection process. In addition, the Second Edition discusses the impact of international regulations governing the conduct of clinical trials and provides guidelines on ensuring compliance with national requirements.Newly featured topics include:\*The growing availability of 'off-the-shelf' solutions for clinical trials\*Potential models for collaboration in the conduct of clinical trials between academia and the pharmaceutical industry\*The increasing use of the Internet in the collection of data and management of trials\*Regulatory requirements worldwide and compliance with the ICH Good Clinical Practice (GCP) Guidelines\*Development of Standard Operating Procedures for the conduct of clinical trialsComplete with chapter summaries that reinforce key points as well as over one hundred examples, Management of Data in Clinical Trials, Second Edition is an ideal resource for practitioners in the clinical research community who are involved in the development of clinical trials, including data managers, research associates, data coordinators, physicians, and statisticians. This book also serves as an excellent supplemental text for courses in clinical trials at both the undergraduate and graduate levels.…

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Hardcover. Condizione: new. Hardcover. A valuable new edition of the trusted, practical guide to managing data in clinical trials Regardless of size, type, or complexity, accurate results for any clinical trial are ultimately determined by the quality of the collected data. Management of Data in Clinical Trials, Second Edition explores data management and trial organization as the keys to developing an accurate and reliable clinical trial. With a focus on the traditional aspects of data collection as well as recent advances in technology, this new edition provides a complete and accessible guide to the management structure of a clinical trial, from planning and development to design and analysis. Practical approaches that result in the collection of complete and timely data are also provided. While maintaining a comprehensive overview of the knowledge and tools that are essential for the organization of a modern clinical trial, the author has expanded the topical coverage in the Second Edition to reflect the possible uses of recent advances in technology in the data collection process. In addition, the Second Edition discusses the impact of international regulations governing the conduct of clinical trials and provides guidelines on ensuring compliance with national requirements. Newly featured topics include: The growing availability of "off-the-shelf" solutions for clinical trialsPotential models for collaboration in the conduct of clinical trials between academia and the pharmaceutical industryThe increasing use of the Internet in the collection of data and management of trialsRegulatory requirements worldwide and compliance with the ICH Good Clinical Practice (GCP) GuidelinesDevelopment of Standard Operating Procedures for the conduct of clinical trials Complete with chapter summaries that reinforce key points as well as over one hundred examples, Management of Data in Clinical Trials, Second Edition is an ideal resource for practitioners in the clinical research community who are involved in the development of clinical trials, including data managers, research associates, data coordinators, physicians, and statisticians. This book also serves as an excellent supplemental text for courses in clinical trials at both the undergraduate and graduate levels. This book explores data management from study development to final analysis and suggests alternative approaches, with guidelines on optimal approaches under various circumstances. It contains discussions of the various approaches to clinical trials for some of the major diseases. This second edition compares approaches in the U.S. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.…

Hardcover. Condizione: Brand New. 2nd edition. 190 pages. 9.25x6.25x0.50 inches. In Stock. This item is printed on demand.