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...
| Otros Autores: | , |
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| Formato: | Libro electrónico |
| Idioma: | Inglés |
| Publicado: |
Cary, North Carolina :
SAS Institute Inc
2022.
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| Materias: | |
| Ver en Biblioteca Universitat Ramon Llull: | https://discovery.url.edu/permalink/34CSUC_URL/1im36ta/alma991009674733006719 |
Tabla de Contenidos:
- Understanding the industry
- Getting started from the case report form
- Study data tabulation model (SDTM)
- Analysis data model (ADM)
- Case report tabulation data definition (Define-XML)
