Electronic common technical document submission with analysis using R

BACKGROUND: In clinical trial development, it is a critical step to submit applications, amendments, supplements, and reports on medicinal products to regulatory agencies. The electronic common technical document is the standard format to enable worldwide regulatory submission. There is a growing tr...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Yujie, Xiao, Nan, Anderson, Keaven, Zhang, Yilong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Short Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941795/
https://www.ncbi.nlm.nih.gov/pubmed/36169229
http://dx.doi.org/10.1177/17407745221123244

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941795/
https://www.ncbi.nlm.nih.gov/pubmed/36169229
http://dx.doi.org/10.1177/17407745221123244

Ejemplares similares