The CRIS registration data set includes, but not limited to, all the items required by the WHO Trial Registration Data Set.
The WHO data set is the minimum amount of trial information that must appear in a register in order for a given trial to be considered fully registered.
There are 20 items in the WHO data set.

Besides these items, the CRIS requires addition information such as information regarding Institutional Review Board approval and participating study sites.

This additional information is required to confirm existence of a study or provide more useful information for the public.
For the details on the CRIS registration data set, please click the download button below.