An Introduction to Creating Standardized Clinical Trial Data with SAS Book Reviews

AUTHOR
Todd Case & YuTing Tian
SCORE
0
TOTAL RATINGS
84

An Introduction to Creating Standardized Clinical Trial Data with SAS by Todd Case & YuTing Tian Book 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.

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Book Name An Introduction to Creating Standardized Clinical Trial Data with SAS
Genre Computers
Published
Language English
E-Book Size 16.32 MB

An Introduction to Creating Standardized Clinical Trial Data with SAS (Todd Case & YuTing Tian) Book Reviews 2024

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Summary of An Introduction to Creating Standardized Clinical Trial Data with SAS by Todd Case & YuTing Tian

The An Introduction to Creating Standardized Clinical Trial Data with SAS book written by Todd Case & YuTing Tian was published on 17 August 2022, Wednesday in the Computers category. A total of 84 readers of the book gave the book 0 points out of 5.

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