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Discussion Framework for Clinical Trial Data Sharing

of therapies and clinical interventions on a firmer basis and enhancing the benefits of clinical trials. Ultimately, such data sharing - if carried out;

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Sharing Clinical Trial Data

in clinical trials or otherwise harm public health. Sharing Clinical Trial Data presents activities and strategies for the responsible sharing;

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Responsible Genomic Data Sharing

Matchmaker Exchange, are discussed in-depth, illuminating pathways forward for new genomic data sharing efforts across research and clinical practice;

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Sharing Clinical Research Data

large and heterogeneous datasets. This public workshop focused on strategies to facilitate sharing of clinical research data in order to advance;

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Developing a National Registry of Pharmacologic and Biologic Clinical Trials

, comprehensive, and transparent registry of relevant information on clinical trials for drugs and biologics. The public and various entities within the;

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Review of the Fialuridine (FIAU) Clinical Trials

of Health and Human Services, the IOM committee has analyzed the FIAU clinical trials, making recommendations for additional safeguards for the;

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Clinical Trials

publication for device and drug trials are also discussed. Clinical Trials provides a comprehensive resource on clinical trials in surgery;

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Fundamentals of Clinical Trials

, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical trial and;

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Fundamentals of Clinical Trials

, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical trial and;

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Data Monitoring Committees in Clinical Trials

decision-making. * Presents practical advice for those managing and conducting clinical trials and serving on Data Monitoring Committees;

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Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law

This book draws a unique perspective on the regulation of access to clinical trial data as a case on research and knowledge externalities;

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Risk-Based Monitoring and Fraud Detection in Clinical Trials Using JMP and SAS

of a clinical trial), prone to error, and limited in its ability to provide insight for data trends across time, patients, and clinical sites;

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Randomised Clinical Trials - Design, Practice & Reporting, 2nd Edition

Clinical Trials is essential reading for clinicians, nurses, data managers, and medical statisticians involved in clinical trials, and for health;

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An Assessment of the NIH Women's Health Initiative

References Appendix A: Clinical Trial Exclusion Criteria Appendix B: U.S. House of Representatives Appropriations COmmittee Appendix C: Statement;

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Management Of Data In Clinical Trials

, accurate results for any clinical trial are ultimately determined by the quality of the collected data. Management of Data in Clinical Trials;

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Practical Guide to Clinical Data Management

The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the;

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Innovation in Clinical Trial Methodologies

-Engineering Clinical Trials that feature innovative options and methods in clinical trials. The Coronavirus pandemic is an accelerator for;

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Clinical Trial Data Analysis Using R and SAS

of biostatistical analyses of clinical trial data with step-by-step implementations using R and SAS. The book's practical, detailed approach draws on the;

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Clinical Trial Data Analysis Using R and SAS

analyses of clinical trial data with step-by-step implementations using R and SAS. The book's practical, detailed approach draws on the authors' 30;

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Improving the Quality of Cancer Clinical Trials

Institute of Medicine committee that will develop consensus-based recommendations for moving the field of cancer clinical trials forward. Table;

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SAS Programming in the Pharmaceutical Industry

This real-world reference for clinical trial SAS programming is packed with solutions that can be applied to day-to-day problems. Organized;

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Implementing CDISC Using SAS

For decades researchers and programmers have used SAS to analyze, summarize, and report clinical trial data. Now Chris Holland and Jack;

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Implementing CDISC Using SAS

For decades researchers and programmers have used SAS to analyze, summarize, and report clinical trial data. Now Chris Holland and Jack;

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Analyzing Longitudinal Clinical Trial Data: A Practical Guide

Analyzing Longitudinal Clinical Trial Data: A Practical Guide provides practical and easy to implement approaches for bringing the latest;

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Analyzing Longitudinal Clinical Trial Data: A Practical Guide

Analyzing Longitudinal Clinical Trial Data: A Practical Guide provides practical and easy to implement approaches for bringing the latest;

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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development

procedures based on accrued data of ongoing clinical trials. The book also gives a well-balanced summary of current regulatory perspectives;

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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development

procedures based on accrued data of ongoing clinical trials. The book also gives a well-balanced summary of current regulatory perspectives. The;

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