The Statistical Programming team at GoBroad Clinical Research Center is a benchmark professional team with extensive experience in regulatory submissions to various regulatory agencies (FDA, EMA, PMDA, CDE, etc.). Their responsibilities include preparing submission data package conforming to SDTM and ADaM standards, annotated CRFs, and preparing relevant submission documents. CDISC standards are currently the default standards at GoBroad Clinical Research Center. Additionally, the technology team develop robust automation platform and rigorously validated systematic tools to facilitate statistical analysis, enhancing both efficiency and quality of statistical analysis.