This course provides training for standards and study administrators.
- create and manage CDISC standards
- create and manage clinical studies
- create CDISC standard SDTM domains
- create Define-XML files for CDSIC clinical submissions.
Who Can Benefit
- Standards administrators and study administrators
- Before attending this course, you should
- be familiar with clinical studies
- have some knowledge of the process of preparing CDISC clinical study submissions
- complete the SAS(R) Drug Development Essentials course.