An introduction to creating standardized clinical trial data with SASĀ®
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...
| Main Authors: | , |
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| Format: | eBook |
| Language: | English |
| Published: |
Cary, North Carolina :
SAS Institute Inc.,
2022.
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| Subjects: | |
| Online Access: | Connect to the full text of this electronic book |
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)