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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. 

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