An introduction to creating standardized clinical trial data with SAS®

An indispensable guide for statistical programmers in the pharmaceutical industry. Statistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical Data Interchange Standards Consortium (CDISC). This book introduces the...

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Bibliographic Details
Call Number:Libro Electrónico
Main Authors: Case, Todd (Author), Tian, YuTian (Author)
Format: Electronic eBook
Language:Inglés
Published: Cary, North Carolina : SAS Institute Inc., 2022.
Subjects:
SAS (Computer file)
Clinical trials > Design.
Clinical trials > Statistical methods.
SAS (Computer program language)
Electronic books.
Online Access:Texto completo (Requiere registro previo con correo institucional)
Table of Contents:
  • Understanding the industry
  • Getting started from the case report form
  • Study data tabulation model (SDTM)
  • Analysis data model (ADM)
  • Case report tabulation data definition (Define-XML)

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