Human Subject Research

Human Research Protection Office & IRBs

All human subject research must be approved by the Institutional Review Board (IRB).

Human subject data should not be collected prior to IRB approval or during expiration gaps. Any data collected prior to approval or while the protocol is expired should be excluded from the study analysis and/or publications.

All research personnel must have a current Conflict of Interest and Good Clinical Practice certification in rascal. Training is available online at the Rascal website.