Main Percent of Office of In Vitro Diagnostics and Radiological Health (OIR) intra- and inter-Office eConsults completed on time during the month CDRH uses the internal expert consultation process to acquire information and analysis on issues related to medical devices. Intra- and inter-office consultations are completed for a variety of work products requiring expertise within and across CDRH offices, including premarket device submissions, post-approval studies, and compliance and enforcement actions. Inter-office eConsults are used to facilitate the exchange of scientific information and staff expertise across CDRH, critical to making well-supported regulatory decisions. eConsult is the system CDRH uses to manage and monitor expert consult requests. <i>Information is current as of December 31, 2012</i> Percent line 0 100 2011 Target FY 2011 Overall: 95% 0 100 2012 FY 2012 Overall: 95% 0 100 2013 FY 2013 YTD: 93% Sub Percent of Office of In Vitro Diagnostics and Radiological Health (OIR) intra- and inter-Office eConsults completed on time during the month Number of OIR intra- and inter-Office eConsults completed on time during the month Number column 0 400 2011 Target FY 2011 Total: 2,795 0 400 2012 FY 2012 Total: 3,042 0 400 2013 FY 2013 YTD: 724 Sub Percent of Office of In Vitro Diagnostics and Radiological Health (OIR) intra- and inter-Office eConsults completed on time during the month Total number of OIR intra- and inter-Office eConsults completed during the month Number column 0 400 2011 Target FY 2011 Total: 2,939 0 400 2012 FY 2012 Total: 3,187 2013 FY 2013 YTD: 781 http://www.fda.gov/AboutFDA/Transparency/track/ucm203038.htm FDA-TRACK CDRH Dashboard track?program=cdrh&id=CDRH-All-Percent-intra-and-inter-office-eConsults-on-time Percent of CDRH intra- and inter-Office eConsults completed on time during the month ਍††਍਍਍਍਍਍਍