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Statistics in Drug Research: Methodologies and Recent Developments (Bog, Hardback, Engelsk)Emphasizing the role of good statistical practices (GSP) in drug research and formulation, this book outlines important statistics... Læs mere
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Genomic Clinical Trials and Predictive Medicine (Bog, Paperback / softback, Engelsk)This book focuses on novel approaches that provide a reliable basis for identifying which patients are likely to benefit from each treatment. Aimed at... Læs mere
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CRC Handbook of Sample Size Guidelines for Clinical Trials (Bog, Hardback, Engelsk)This volume helps medical researchers design clinical trials to improve survival, remission duration, or time to recurrence of... Læs mere
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Handbook of Statistics in Clinical Oncology (Bog, Paperback / softback, Engelsk)The third edition presents up-to-date statistical approaches to the design and analysis of oncology clinical trials. New topics include trial designs for... Læs mere
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Design and Analysis of Clinical Trials with Time-to-Event Endpoints (Bog, Paperback / softback, Engelsk)Levering: 6 - 9 hverdage -
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Monte Carlo Simulation for the Pharmaceutical Industry: Concepts, Algorithms, and Case Studies (Bog, Paperback / softback, Engelsk)Levering: Skaffevare (forvent 14 - 30 hverdage) -
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Theory of Drug Development (Bog, Paperback / softback, Engelsk)Levering: Skaffevare (forvent 14 - 30 hverdage) -
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Introduction to Randomized Controlled Clinical Trials (Bog, Hardback, Engelsk)Focusing on the important role that statistical methods play in the analysis of the data collected as well as in the overall clinical trial process,... Læs mere
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Toxicity and Risk: Context, Principles and Practice (Bog, Hardback, Engelsk)This book aims to set out the political, social, legal and scientific underpinning of risk assessment and risk management for toxic substances. It describes the principles and processes the practitioners undertake when looking at the regulatory risk implications of their work.
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Design and Analysis of Quality of Life Studies in Clinical Trials (Bog, Hardback, Engelsk)Presents a range of solutions to analytic issues. This title reflects developments in methodology with coverage of mixture models and a... Læs mere
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Design and Analysis of Clinical Trials with Time-to-Event Endpoints (Bog, Hardback, Engelsk)Provides a presentation of the design, monitoring, analysis, and interpretation of clinical trials in which time-to-event is of critical interest. This book discusses the design and monitoring of Phase II and III clinical trials with time-to-event endpoints.
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Randomized Clinical Trials of Nonpharmacological Treatments (Bog, Hardback, Engelsk)Levering: Skaffevare (forvent 14 - 30 hverdage)
