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Zustand: Good. 1st Edition. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

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hardcover. Zustand: Very Good.

hardcover. Zustand: Gut. 208 Seiten; 9780471489863.3 Gewicht in Gramm: 500.

hardcover. Zustand: New. In shrink wrap. Looks like an interesting title.

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Hardback. Zustand: New. ­The authoritative guide for Data Monitoring Committees-fully revised and updated The number of clinical trials sponsored by government agencies and pharmaceutical companies has grown in recent years, prompting an increased need for interim monitoring of data on safety and efficacy. Data Monitoring Committees (DMCs) are an essential component of many clinical trials, safeguarding trial participants and protecting the credibility and validity of the study. Data Monitoring Committees in Clinical Trials: A Practical Perspective, 2nd Edition offers practical advice for those managing and conducting clinical trials and serving on Data Monitoring Committees, providing a practical overview of the establishment, purpose, and responsibilities of these committees. Examination of topics such as the composition and independence of DMCs, statistical, philosophical and ethical considerations, and determining when a DMC is needed, presents readers with a comprehensive foundational knowledge of clinical trial oversight. Providing recent examples to illustrate DMC principles, this fully-updated guide reflects current developments and practices in clinical trial oversight and offers expanded coverage of emerging issues and challenges in the field. This new second edition covers the most current information on DMC policies, issues in monitoring trials using new designs, and recent trial publications relevant to DMC decision-making. . Presents practical advice for those managing and conducting clinical trials and serving on Data Monitoring Committees . Illustrates the types of challenging issues Data Monitoring Committees face in practical situations . Provides updated and expanded coverage of topics including regulatory and funding agency guidelines and trial designs and their associated demands and limitations . Includes a new chapter addressing legal issues that affect DMC members and discusses general litigation concerns relevant to clinical research . Expands treatment of current journal publications addressing DMC issues Data Monitoring Committees in Clinical Trials: A Practical Perspective, 2nd Edition is a must-have text for anyone engaged in DMC activities as well as trial sponsors, clinical trial researchers, regulatory and bioethics professionals, and those associated with clinical trials in academic, government and industry settings.…

hardcover. Zustand: Sehr gut. Auflage: 1. 208 Seiten minimale Stauchung am seitlichen Coverrand, kleine Lagerspuren am Buch, Inhalt einwandfrei und ungelesen Sprache: Englisch Gewicht in Gramm: 430.

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Zustand: New. 2019. Hardcover. . . . . .

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Hardcover. Zustand: Brand New. 2nd edition. 496 pages. 9.00x6.30x1.10 inches. In Stock.

Zustand: New. 2019. Hardcover. . . . . . Books ship from the US and Ireland.

Hardback. Zustand: New. ­The authoritative guide for Data Monitoring Committees-fully revised and updated The number of clinical trials sponsored by government agencies and pharmaceutical companies has grown in recent years, prompting an increased need for interim monitoring of data on safety and efficacy. Data Monitoring Committees (DMCs) are an essential component of many clinical trials, safeguarding trial participants and protecting the credibility and validity of the study. Data Monitoring Committees in Clinical Trials: A Practical Perspective, 2nd Edition offers practical advice for those managing and conducting clinical trials and serving on Data Monitoring Committees, providing a practical overview of the establishment, purpose, and responsibilities of these committees. Examination of topics such as the composition and independence of DMCs, statistical, philosophical and ethical considerations, and determining when a DMC is needed, presents readers with a comprehensive foundational knowledge of clinical trial oversight. Providing recent examples to illustrate DMC principles, this fully-updated guide reflects current developments and practices in clinical trial oversight and offers expanded coverage of emerging issues and challenges in the field. This new second edition covers the most current information on DMC policies, issues in monitoring trials using new designs, and recent trial publications relevant to DMC decision-making. . Presents practical advice for those managing and conducting clinical trials and serving on Data Monitoring Committees . Illustrates the types of challenging issues Data Monitoring Committees face in practical situations . Provides updated and expanded coverage of topics including regulatory and funding agency guidelines and trial designs and their associated demands and limitations . Includes a new chapter addressing legal issues that affect DMC members and discusses general litigation concerns relevant to clinical research . Expands treatment of current journal publications addressing DMC issues Data Monitoring Committees in Clinical Trials: A Practical Perspective, 2nd Edition is a must-have text for anyone engaged in DMC activities as well as trial sponsors, clinical trial researchers, regulatory and bioethics professionals, and those associated with clinical trials in academic, government and industry settings.…

Hardcover. Zustand: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

paperback. Zustand: New. Paperback. Pub Date: 2020-12-01 Pages: 364 Language: Chinese Publisher: Peking University Medical Press. In recent years. the number of clinical trials funded by government agencies and pharmaceutical companies has been increasing. which has allowed for the The demand for mid-term audits continues to rise.?The Data Monitoring Committee (DMC) is an essential part of many clinical trials. which can protect the safety of trial subjects and maintain the integrity and credibility of the research...…