Staff blinding is an important part of clinical trials that randomize subjects to various treatment arms.

The blinding module can be enabled in the project settings, and has an impact on what a project member can see.

Blinded project members cannot randomize subjects or report adverse events, and also cannot see existing subject randomizations, adverse events, restricted designs, or comments on restricted designs.

Please note that the project owner must be unblinded. Project ownership can be transferred to another staff member via the project settings if this is not the case.

For projects that don't have blinding enabled, all project members are considered unblinded.