An Introduction to Creating Standardized Clinical Trial Data with SAS
Language: English
Published by SAS Institute, 2022
- Softcover
- New
Condition: New
£ 47.07
Quantity: Over 20 available
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Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. KlappentextrnrnAn indispensable guide for statistical programmers in the pharmaceutical industry.nnnStatistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical.
Seller Inventory # 701158747
- Title
- An Introduction to Creating Standardized Clinical Trial Data with SAS
- Author
- Case, Todd|Tian, Yuting
- Publisher
- SAS Institute
- Publication year
- 2022
- Condition
- New
- Binding
- Soft cover
- Language
- English
- ISBN 10
- 195597795X
- ISBN 13
- 9781955977951
- Seller catalogs
- Importe
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.
"Synopsis" may belong to another edition of this title.
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