From the ACCME:
We are in the process of making modifications to PARS to accommodate REMS activities. Until PARS is ready, we have been using a hybrid of the current PARS database and a supplemental spreadsheet to compile the data requested by the FDA. We are not yet collecting data on activities that are Related to Regulation – just those that are REMS-compliant (and RPC-funded). Once PARS is built out to accommodate REMS, our data collection capabilities will be greater. We have not encountered any technical issues related to this project.