Search Results - Data Interpretation, Statistical.

Surrogate endpoints, part 1 from definition to meta-analytic framework /

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Surrogate endpoints, part 2 further developments /

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Treatment effect estimates in multi-arm multi-stage (MAMS) clinical trials

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Design and conduct of non-inferiority trials

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Series (Risk of bias in randomized clinical trials)
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Interface between regulation and statistics in drug development / by Alemayehu, Demissie, Emir, Birol, Gaffney, Michael, active 1983

Table of Contents: “…Cover -- Half Title -- Series Information -- Title Page -- Copyright Page -- Table of contents -- Figures -- Abbreviations -- Authors' Disclosure -- Acknowledgment -- Preface -- About the Authors -- Chapter 1 Fundamental Principles of Clinical Trials -- 1.1 Introduction -- 1.2 General Statistical Considerations -- 1.2.1 Statistical Analysis Plan -- 1.2.2 Trial Design -- 1.2.3 Randomization and Blinding -- 1.2.4 Statistical Methodology -- 1.2.5 Reporting and Interpretation of Study Results -- 1.2.6 Data Quality and Software Validity -- 1.3 Evolving Roles of the Statistician in Drug Development…”
Taylor & Francis
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