As understood, in the process to amplify data’s impact, CDISC helps to drive clarity in clinical research. This is achieved significantly by bringing together a global community of experts to develop and advance data standards of the highest quality.
SCL IT collaborates with the bio-pharma industry to enable accessibility, interoperability, and reusability of data for more meaningful and efficient research that has greater impact on global health
SCL IT offers the needful expert advice on all aspects of CDISC therapeutic area standards. This includes,
- Guidance on which domains and datasets to use in collecting and storing data
- Guidance on which variables to use to represent data items
- Guidance on the definition of non-standard (supplemental) variables, when the currently defined standard variables are insufficient for the task
- Guidance on relating data across domains and datasets