Statistical thinking for non-statisticians in drug regulation / Richard Kay, PhD, Statistical Consultant, RK Statistics Ltd, Honorary Visiting Professor, School of Pharmacy, Cardiff University, UK.

Author/creator Kay, R., 1949-
Format Electronic
EditionSecond edition.
Publication InfoChichester, West Sussex, UK ; Hoboken, New Jersey : Wiley Blackwell, 2015.
Description1 online resource.
Supplemental ContentFull text available from Ebook Central - Academic Complete
Subjects

Contents Basic ideas in clinical trial design -- Sampling and inferential statistics -- Confidence intervals and p-values -- Tests for simple treatment comparisons -- Adjusting the analysis -- Regression and analysis of covariance -- Intention-to-treat and analysis sets -- Power and sample size -- Statistical significance and clinical importance -- Multiple testing -- Non-parametric and related methods -- Equivalence and non-inferiority -- The analysis of survival data -- Interim analysis and data monitoring committees -- Bayesian statistics -- Adaptive designs -- Observational studies -- Meta-analysis -- Methods for the safety analysis and safety monitoring -- Diagnosis -- The role of statistics and statisticians.
Bibliography noteIncludes bibliographical references and index.
Access restrictionAvailable only to authorized users.
Technical detailsMode of access: World Wide Web
Source of descriptionDescription based on print version record and CIP data provided by publisher.
Issued in other formPrint version: Kay, R. (Richard), 1949- author. Statistical thinking for non-statisticians in drug regulation Second edition. Chichester, West Sussex, UK ; Hoboken, NJ, USA : John Wiley & Sons Inc., 2015 9781118470947
Genre/formElectronic books.
LCCN 2014021547
ISBN9781118470978 (ePub)
ISBN9781118470992 (Adobe PDF)

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Electronic Resources Access Content Online ✔ Available