If your IRB is already registered in the OHRP system, the registration information must be
updated to include all of the information required by FDA (see # 11 below). For IRBs that are
currently reviewing FDA-regulated research, the additional information must be added to the
database by September 14, 2009. For IRBs that are not currently reviewing FDA-regulated
research, this must be done before any research involving FDA-regulated products is reviewed
once the compliance date has passed.
