Planning pharmaceutical clinical trials : basic statistical principles /

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Bibliographic Details
Author / Creator:Wooding, William M.
Imprint:New York : J. Wiley & Sons, c1994.
Description:xx, 539 p. : ill. ; 25 cm.
Language:English
Series:Wiley series in probability and mathematical statistics. Applied probability and statistics
Subject:Drugs -- Testing -- Planning.
Drugs -- Testing -- Statistical methods.
Drug Evaluation -- methods
Clinical Trials -- methods
Research Design
Statistics as Topic
Drugs -- Testing -- Statistical methods.
Format: Print Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/1622867
Hidden Bibliographic Details
ISBN:0471622443 (cloth : alk. paper)
Notes:"A Wiley-Interscience publication."
Includes bibliographical references (p. 518-529) and index.
Table of Contents:
  • Pt. I. Preliminary Considerations
  • Ch. 1. Introduction. Ch. 2. Nature and Purposes of Clinical Testing. Ch. 3. The Role of the FDA
  • Pt. II. Planning Your Trial. Ch. 4. Planning Your Trial: I. Ch. 5. Planning Your Trial: II. Ch. 6. Planning Your Trial: III. Ch. 7. The Protocol and Clinical Report Forms
  • Pt. III. Some Experimental Designs, with Examples. Ch. 8. One-Factor Parallel Designs. Ch. 9. Multifactor Parallel Designs. Ch. 10. Parallel Factorial Designs: Examples. Ch. 11. Parallel Factorial Designs: Blocking. Ch. 12. Changeover Designs
  • Pt. IV. Basic Statistical Analysis. Ch. 13. Data Analysis: Fundamental Ideas. Ch. 14. Data Analysis: Basic Statistical Procedures
  • Pt. V. Details of Sample Size Estimation. Ch. 15. Sample Size Estimation. App. A.1 Explanation and Discussion of Tables and Programs
  • App. A.2 Tables and Programs.