ISBN: 9781955977982 - an introduction to creating standardized clinical trial data with sas (16 risultati)

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Condizione: Very Good. : Esta obra constituye una guía indispensable para los programadores estadísticos que trabajan en la industria farmacéutica. El libro introduce los conceptos fundamentales, el conocimiento específico del sector y las prácticas de programación en SAS necesarias para cumplir con las normativas del Consorcio de Estándares de Intercambio de Datos Clínicos (CDISC).A través de explicaciones claras y ejemplos prácticos, el lector aprenderá a estructurar datos en cada etapa del proceso, desde la anotación de formularios electrónicos de reporte de casos (eCRFs) hasta la definición de la relación entre SDTM y ADaM, incluyendo la generación de archivos Define-XML para la transmisión de metadatos. Es un recurso esencial para programadores de nivel inicial que buscan alcanzar el éxito profesional en este campo altamente regulado. EAN: 9781955977982 Tipo: Libros Categoría: Tecnología|Ciencias Título: An Introduction to Creating Standardized Clinical Trial Data with SAS Autor: Todd Case| YuTing Tian Idioma: en Páginas: 238 Formato: Tapa dura Año de publicación: 2022.…

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Hardcover. Condizione: Brand New. 240 pages. 7.50x0.56x9.25 inches. In Stock.

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Gebunden. Condizione: New. 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.…

Buch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - 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.…

Buch. Condizione: Neu. An Introduction to Creating Standardized Clinical Trial Data with SAS | Todd Case (u. a.) | Buch | Englisch | 2022 | SAS Institute | EAN 9781955977982 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu Print on Demand.…