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Data Monitoring Committees in Clinical Trials

The authoritative guide for Data Monitoring Committees-fully revised and updated The number of clinical trials sponsored by government;

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Data and Safety Monitoring Committees in Clinical Trials

Focusing on the practical clinical and statistical issues that arise in pharmaceutical industry trials, this book summarizes the author's;

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Data and Safety Monitoring Committees in Clinical Trials

data monitoring committees (DMCs). Maintaining all the material from the first edition and adding substantial new material, Data and Safety;

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

guidelines recommend that clinical trial data should be actively reviewed or monitored; the well-being of trial participants and the validity and;

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Clinical Trials

underlying principles of clinical trials, trial design, the development of a study cohort, statistics, data safety, data monitoring, and trial;

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Statistical Design, Monitoring, and Analysis of Clinical Trials: Principles and Methods

Statistical Design, Monitoring, and Analysis of Clinical Trials, Second Edition concentrates on the biostatistics component of clinical;

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Analysis of Clinical Trials Using SAS

trials, including analysis of stratified data, incomplete data, multiple inferences, issues arising in safety and efficacy monitoring, and;

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Analysis of Clinical Trials Using SAS

trials, including analysis of stratified data, incomplete data, multiple inferences, issues arising in safety and efficacy monitoring, and;

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Analysis of Clinical Trials Using SAS

trials, including analysis of stratified data, incomplete data, multiple inferences, issues arising in safety and efficacy monitoring, and;

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Clinical Trials in Cancer

Clinical Trials in Cancer provides concise, accessible and practical information on the practicalities of planning, designing, conducting;

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Clinical Trials Handbook

A systematic approach to all aspects of designing and conducting clinical trials The success or failure of clinical trials hinges on;

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Fundamental Concepts for New Clinical Trialists

versus crossover designs; data monitoring; analyses of efficacy, safety, and benefit-risk; and the reporting/publication of clinical trial;

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Fundamental Concepts for New Clinical Trialists

versus crossover designs; data monitoring; analyses of efficacy, safety, and benefit-risk; and the reporting/publication of clinical trial;

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Clinical Trials Handbook

effectiveness and safety for public use. They require intensive planning and organization and involve a wide range of disciplines: data management;

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Statistical Design and Analysis of Clinical Trials

Students How to Design, Monitor, and Analyze Clinical Trials The book begins with ethical and safety principles, core trial design concepts, the;

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Quantitative Evaluation of Safety in Drug Development

clinical trials and observational studies in biopharmaceutical product development. It presents the latest statistical methods for drug safety;

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

and stepped wedge trials. Other new chapters describe data and safety monitoring, biomarker studies, and feasibility studies. Updated and;

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Statistics Applied to Clinical Trials

in the planning and conducting of clinical trials. As a consequence, prior to approval, clinical trial protocols are now routinely scrutinized by;

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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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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development

In response to the US FDA's Critical Path Initiative, innovative adaptive designs are being used more and more in clinical trials due to;

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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development

In response to the US FDA's Critical Path Initiative, innovative adaptive designs are being used more and more in clinical trials due to;

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Oncology Clinical Trials

of conducting and analyzing cancer clinical trials in the era of precision medicine with biologic agents-including trials investigating the safety and;

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Data Monitoring in Clinical Trials: A Case Studies Approach

From the authors of Fundamentals of Clinical Trials which has sold over 15,000 copies world wide since its publication in 1998. No;

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Statistics Applied to Clinical Trials

for circumspection in planning and conducting of clinical trials. As a consequence, prior to approval, clinical trial protocols are now;

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Design and Analysis of Clinical Trials with Time-To-Event Endpoints

, number of events, and independence or noninformativeness of the censoring mechanisms relative to the event. Design and Analysis of Clinical;

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Dictionary for Clinical Trials

This is a unique and comprehensive book providing clearly written definitions of the clinical trial terms likely to be found in trial;

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