An Introduction to Creating Standardized Clinical Trial Data with SAS

Case, Todd/ Tian, YuTing

ISBN 10: 195597795X / ISBN 13: 9781955977951

Published by SAS Institute, 2022

About this Item

238 pages. 9.25x7.50x0.54 inches. In Stock.

Seller Inventory # x-195597795X

Bibliographic Details

• Title: An Introduction to Creating Standardized Clinical Trial Data with SAS
• Publisher: SAS Institute
• Publication Date: 2022
• Language: English
• ISBN 10: 195597795X
• ISBN 13: 9781955977951
• Binding: Paperback
• Condition: Brand New
• Weight: 0.53 kilograms

About this title

Synopsis

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.