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

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