Ir directamente a la navegación principal Ir directamente a la búsqueda Ir directamente al contenido principal

Development of data validation rules for therapeutic area standard data elements in four mental health domains to improve the quality of FDA submissions

Producción científica: Chapter

Resumen

Data standards are now required for many submissions to the United States Food and Drug Administration (FDA). The required standard for submission of clinical data is the Clinical Data Interchange Standards Consortium (CDISC) Submission Data Tabulation Model (SDTM). Currently, 45 business rules and 115 associated validation rules exist for SDTM data. However, such rules have not yet been developed for therapeutic area data standards developed under the last reauthorization of the Prescription Drug User Fee Act (PDUFA V). The objective of this effort was to develop data validation rules for new therapeutic area data standards in four mental health domains, assess the metadata required to associate such rules with standard data elements, and assess the level of data validation possible for therapeutic area data elements.

Idioma originalEnglish (US)
Título de la publicación alojadaImproving Usability, Safety and Patient Outcomes with Health Information Technology
Subtítulo de la publicación alojadaFrom Research to Practice
EditoresAlex Mu-Hsing Kuo, Andre Kushniruk, Francis Lau, Elizabeth M. Borycki, Gerry Bliss, Helen Monkman, Abdul Vahabpour Roudsari, John A. Bartle-Clar, Karen L. Courtney
EditorialIOS Press
Páginas125-132
Número de páginas8
ISBN (versión digital)9781614999508
DOI
EstadoPublished - 2019
Publicado de forma externa

Serie de la publicación

NombreStudies in Health Technology and Informatics
Volumen257
ISSN (versión impresa)0926-9630
ISSN (versión digital)1879-8365

ASJC Scopus subject areas

  • Biomedical Engineering
  • Health Informatics
  • Health Information Management

Huella

Profundice en los temas de investigación de 'Development of data validation rules for therapeutic area standard data elements in four mental health domains to improve the quality of FDA submissions'. En conjunto forman una huella única.

Citar esto