rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Strategy and statistics in clinical trials
    sub title: a non-statisticians guide to thinking, designing, and executing
  name:
    name part: Tal, Joseph.
    role:
      role term: creator
  name:
    name part: ScienceDirect (Online service)
  type of resource: text
  genre: Electronic books.
  origin info:
    place:
      place term: mau
    date issued: 2011
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: remote
    extent: 1 online resource.
  abstract: Strategy and Statistics in Clinical Trials is for all individuals engaged in clinical research, including professors, physicians, researchers in corporate and government laboratories, nurses, members of the allied health professions, and post-doctoral and graduate students who are potentially less exposed to understanding the pivotal role of statistics. . Enables nonstatisticians to better understand research processes and statistics' role in these processes . Offers real-life case studies and provides a practical, "how to" guide to biomedical R&D . Delineates the statistical building blocks and concepts of clinical trials . Promotes effective cooperation between statisticians and important other parties.
  table of contents: Chapter 1.) Clinical Development and Statistics: The General View Chapter 2.) Questions when Planning Trials Chapter 3.) Medical Product Attributes Chapter 4.) Setting Research Objectives Chapter 5.) Statistical Thinking Chapter 6.) Estimation Chapter 7.) From Description to Testing: A Beginning Chapter 8.) Statistical Significance, Explanation and Prediction Chapter 9.) Exploratory and Confirmatory Clinical Trials Chapter 10.) One, Two, Three Testing: Hypothesis Testing and Multiplicity Chapter 11.) Elements of Clinical Trial Design I: Putting it together Chapter 12.) Elements of Clinical Trial Design II Chapter 13.) Choosing Trial Endpoints Chapter 14.) Determination of Sample Size Chapter 15.) Concluding Remarks.
  note: Joseph Tal.
  note: Machine generated contents note: Chapter 1.) Clinical Development and Statistics: The General View Chapter 2.) Questions when Planning Trials Chapter 3.) Medical Product Attributes Chapter 4.) Setting Research Objectives Chapter 5.) Statistical Thinking Chapter 6.) Estimation Chapter 7.) From Description to Testing: A Beginning Chapter 8.) Statistical Significance, Explanation and Prediction Chapter 9.) Exploratory and Confirmatory Clinical Trials Chapter 10.) One, Two, Three Testing: Hypothesis Testing and Multiplicity Chapter 11.) Elements of Clinical Trial Design I: Putting it together Chapter 12.) Elements of Clinical Trial Design II Chapter 13.) Choosing Trial Endpoints Chapter 14.) Determination of Sample Size Chapter 15.) Concluding Remarks.
  note: Electronic resource.
  subject:
    topic: Clinical trials
    topic: Statistical methods
  classification: R853.C55 T35 2011
  classification: 615.5072/4
  related item:
    title info:
      title: Strategy and statistics in clinical trials
    name:
      name part: Tal, Joseph.
    origin info:
      publisher: Burlington, MA : Academic Press, 2011
    identifier: (DLC) 2011009725
    identifier: (OCoLC)693812429
  identifier: 9780123869098 (electronic bk.)
  identifier: 0123869099 (electronic bk.)
  identifier: 1105931:10989071 Elsevier Science & Technology
  identifier: http://proxy.library.tamu.edu/login
  record info:
    record content source: OPELS
    record creation date: 110803
    record change date: 20260609193548.5
    record identifier: in00002708224
    language of cataloging:
      language term: eng