Statistical methodology in the pharmaceutical sciences

Contributor(s):

Berry, Donald A [Editor]

Material type: Text

TextSeries: Publication details: New York M. Dekker 1990Description: viii, 578 pISBN:

9780824781170

Subject(s):

DDC classification:

615.1901 S8

Summary: A state-of-the-art handbook of statistical analysis for use in the pharmaceutical industry. Areas covered in this reference/text include: bioavailability, repeated-measures designs, dose-response, population models, multicenter trials, handling dropouts, survival analysis, robust data analysis, cate. Table of content: Basic principles in designing and analyzing clinical studies / Donald A. Berry Bioavailability : designs and analysis / Bruce E. Rodda Analysis of repeated-measures designs / George A. Milliken Dose-response : relating doses and plasma levels to efficacy and adverse experiences / Bruce P. Ekholm, Terrance L. Fox, and James A. Bolognese Population models / Amy Racine-Poon and Adrian F.M. Smith Linear and nonlinear regression / R. Dennis Cook and Sanford Weisberg Design and analysis of multicenter trials / Judith D. Goldberg and Kenneth J. Koury Crossover versus parallel designs / Andrew P. Grieve. Handling dropouts and related issues / Richard G. Cornell Group sequential methods in clinical trials / Peter C. O'Brien Survival analysis / John D. Kalbfleisch and James O. Street Robust data analysis / Robert V. Hogg, Stephen J. Ruberg, and Lianng Yuh Categorical data analysis / Gary G. Koch ... [et al.] Causality assessment for adverse drug reactions / David A. Lane Bayesian metaanalysis / William DuMouchel Inferential problems in postmarketing surveillance / David A. Lane and Nigel S.B. Rawson. (https://openlibrary.org/works/OL5374202W/Statistical_Methodology_in_the_Pharmaceutical_Sciences_%28Statistics_a_Series_of_Textbooks_and_Monogrp)

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Item type	Current library	Collection	Call number	Status	Date due	Barcode	Item holds
Book	Ahmedabad	Non-fiction	615.1901 S8 (Browse shelf(Opens below))	Available		189681

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Previous	615.10724 D3 Design and analysis of bridging studies	615.19 H2Q8 Quality control training manual: comprehensive training guide for API, finished pharmaceutical and biotechnologies laboratories	615.19 B5B2 Basic principles of drug discovery and development	615.1901 S8 Statistical methodology in the pharmaceutical sciences

A state-of-the-art handbook of statistical analysis for use in the pharmaceutical industry. Areas covered in this reference/text include: bioavailability, repeated-measures designs, dose-response, population models, multicenter trials, handling dropouts, survival analysis, robust data analysis, cate.

Table of content:
Basic principles in designing and analyzing clinical studies / Donald A. Berry
Bioavailability : designs and analysis / Bruce E. Rodda
Analysis of repeated-measures designs / George A. Milliken
Dose-response : relating doses and plasma levels to efficacy and adverse experiences / Bruce P. Ekholm, Terrance L. Fox, and James A. Bolognese
Population models / Amy Racine-Poon and Adrian F.M. Smith
Linear and nonlinear regression / R. Dennis Cook and Sanford Weisberg
Design and analysis of multicenter trials / Judith D. Goldberg and Kenneth J. Koury
Crossover versus parallel designs / Andrew P. Grieve.
Handling dropouts and related issues / Richard G. Cornell
Group sequential methods in clinical trials / Peter C. O'Brien
Survival analysis / John D. Kalbfleisch and James O. Street
Robust data analysis / Robert V. Hogg, Stephen J. Ruberg, and Lianng Yuh
Categorical data analysis / Gary G. Koch ... [et al.]
Causality assessment for adverse drug reactions / David A. Lane
Bayesian metaanalysis / William DuMouchel
Inferential problems in postmarketing surveillance / David A. Lane and Nigel S.B. Rawson.
(https://openlibrary.org/works/OL5374202W/Statistical_Methodology_in_the_Pharmaceutical_Sciences_%28Statistics_a_Series_of_Textbooks_and_Monogrp)

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