An introduction to creating standardized clinical trial data with SAS®

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...

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Detalles Bibliográficos
Otros Autores: Case, Todd, author (author), Tian, YuTian, author
Formato: Libro electrónico
Idioma:Inglés
Publicado: Cary, North Carolina : SAS Institute Inc 2022.
Materias:
Ver en Biblioteca Universitat Ramon Llull:https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009674733006719
Descripción
Sumario: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.
Descripción Física:1 online resource : illustrations
ISBN:9781955977975