It’s a safe bet that most people’s first introduction to CDISC standards is through the Study Data Tabulation Model (SDTM). This is a content standard that ensures clinical data is submitted in a ...

Global RBM requires interoperable architectures across EDC, IRT, eCOA, labs, imaging, EHR, and safety systems, but inconsistent CDISC/HL7 FHIR adoption and proprietary APIs impede near–real-time ...

Wake Tech offers workforce training programs for dozens of occupations, and financial assistance may be available for students interested in courses that aren't part of Wake Tech's Propel program.

The Statistical Center for HIV/AIDS Research and Prevention (SCHARP) is part of the Biostatistics, Bioinformatics and Epidemiology (BBE) research program at Fred Hutch Cancer Center and is housed ...

Continuous medical and safety monitoring of subject data during a clinical trial is a critical part of evaluating the safety of trial participants and as such is governed by protocol procedures and ...

The contents of this repository are provided under the Creative Commons Attribution (CC-BY) 4.0 license as laid out in the LICENSE.md file. The R projects in this repository designed for the ...

A Case Report Form (CRF) is a printed, optical, or electronic document designed to record all information required to be reported to the sponsor on each trial subject. CRFs play a crucial role in ...