| Description |
1 online resource : illustrations |
| 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) |
| Summary |
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 basic concepts, pharmaceutical industry knowledge, and SAS programming practices that every programmer needs to know to comply with regulatory requirements. Step-by-step, you will learn how data should be structured at each stage of the process from annotating electronic Case Report Forms (eCRFs) and defining the relationship between SDTM and ADaM, to understanding how to generate a Define-XML file to transmit metadata. Filled with clear explanations and example code, this book focuses only on the essential information that entry-level programmers need to succeed. |
| Subject |
SAS (Computer file)
|
|
SAS (Computer file) |
|
Clinical trials -- Design.
|
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Clinical trials -- Statistical methods.
|
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SAS (Computer program language)
|
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Études cliniques -- Méthodes statistiques. |
|
SAS (Langage de programmation) |
|
Clinical trials -- Design |
|
Clinical trials -- Statistical methods |
|
SAS (Computer program language) |
| Genre |
Electronic books.
|
| Added Author |
Tian, YuTian, author.
|
| ISBN |
1955977976 (electronic bk.) |
|
9781955977975 (electronic bk.) |
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