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Quantitative Evaluation of Safety in Drug Development

Evaluation of Safety in Drug Development: Design, Analysis and Reporting explains design, monitoring, analysis, and reporting issues for both;

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Analysis of Safety Data of Drug Trials: An Update

machine learning clusters and networks, and multivariate analyses. As a result, it is time that an updated version of safety data analysis;

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Post-Authorization Safety Studies of Medicinal Products

novel and advanced design and analysis approaches for causal interference from observational data. This book serves as an important reference;

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

trials. The book then covers areas of drug development, medical practice, and safety assessment. It concludes with the design and analysis;

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Data and Safety Monitoring Committees in Clinical Trials

of safety Use of meta analysis and data outside the trial New ideas for training and compensation of DMC members Jay Herson is Senior Associate;

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Statistical Methods for Drug Safety

selection bias in the analysis of large-scale longitudinal observational data. Choose the Right Statistical Approach for Analyzing Your Drug Safety;

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Statistical Methods for Drug Safety

selection bias in the analysis of large-scale longitudinal observational data. Choose the Right Statistical Approach for Analyzing Your Drug;

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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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Statistics in Drug Research

applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation and;

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Statistics in Drug Research

applications for each stage of pharmaceutical development to ensure the valid design, analysis, and assessment of drug products under investigation and;

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Management of Heart Failure

sections concentrate on a review of screening, assessment and diagnosis; an update on drug treatments; an update on device therapy; and a;

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Bioequivalence and Statistics in Clinical Pharmacology

of clinical pharmacology drug development, regulatory applications, and the design and analysis of bioequivalence trials are established, they move on;

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Clinical Trials

, orphan drugs, biosimilars, drug regulations in Europe, drug safety, regulatory approval and more Extensively covers the "study schema;

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Real-World Evidence in Drug Development and Evaluation

This book concerns use of real world data (RWD) and real world evidence (RWE) to aid drug development across product cycle. RWD are;

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Progress in Neurotherapeutics and Neuropsychopharmacology

series is guided by an editor-in-chief and editorial board with broad experience in drug development and neuropsychopharmacology. Progress;

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Progress in Neurotherapeutics and Neuropsychopharmacology

series is guided by an editor-in-chief and editorial board with broad experience in drug development and neuropsychopharmacology. Progress;

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Design and Analysis of Non-Inferiority Trials

of issues of non-inferiority trials, including multiple comparisons, missing data, analysis population, the use of safety margins, the internal;

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Design and Analysis of Non-Inferiority Trials

-inferiority trials, including multiple comparisons, missing data, analysis population, the use of safety margins, the internal consistency of non;

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Statistical Design and Analysis of Clinical Trials

Statistical Design and Analysis of Clinical Trials: Principles and Methods concentrates on the biostatistics component of clinical trials;

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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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Biomarker Analysis in Clinical Trials with R

pharmaceutical industry on how to incorporate biomarker data analysis in clinical trial studies. The book discusses the appropriate statistical methods;

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Biomarker Analysis in Clinical Trials with R

pharmaceutical industry on how to incorporate biomarker data analysis in clinical trial studies. The book discusses the appropriate statistical methods;

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Progress in Neurotherapeutics and Neuropsychopharmacology

series is guided by an editor-in-chief and editorial board with broad experience in drug development and neuropsychopharmacology. Progress;

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Progress In Neurotherapeutics And Neuropsychopharmacology: V

series is guided by an editor-in-chief and editorial board with broad experience in drug development and neuropsychopharmacology. Progress;

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Progress in Neurotherapeutics and Neuropsychopharmacology

series is guided by an editor-in-chief and editorial board with broad experience in drug development and neuropsychopharmacology. Progress;

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