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U.S. Department of Health and Human Services

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Percent of Office of Surveillance and Biometrics (OSB) intra- and inter-Office eConsults completed on time during the month

Dictionary: 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.

Data is current as of December 31, 2012

Fiscal Year - 2013

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TimeTargetPercent
Oct 20128593
Nov 20128591
Dec 20128592
Jan 201385TBD
Feb 201385TBD
Mar 201385TBD
Apr 201385TBD
May 201385TBD
Jun 201385TBD
Jul 201385TBD
Aug 201385TBD
Sep 201385TBD

FY 2013 YTD: 92%

Number of OSB intra- and inter-Office eConsults completed on time during the month

Fiscal Year - 2013
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TimeTargetNumber
Oct 2012N/A264
Nov 2012N/A230
Dec 2012N/A258
Jan 2013N/ATBD
Feb 2013N/ATBD
Mar 2013N/ATBD
Apr 2013N/ATBD
May 2013N/ATBD
Jun 2013N/ATBD
Jul 2013N/ATBD
Aug 2013N/ATBD
Sep 2013N/ATBD

FY 2013 YTD: 752

Total number of OSB intra- and inter-Office eConsults completed during the month

Fiscal Year - 2013
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TimeTargetNumber
Oct 2012N/A285
Nov 2012N/A254
Dec 2012N/A280
Jan 2013N/ATBD
Feb 2013N/ATBD
Mar 2013N/ATBD
Apr 2013N/ATBD
May 2013N/ATBD
Jun 2013N/ATBD
Jul 2013N/ATBD
Aug 2013N/ATBD
Sep 2013N/ATBD

FY 2013 YTD: 819

Glossary

Note: The data provided on this website is produced on an ongoing basis for performance management purposes and is subject to change due to updates of preliminary estimates, corrections, or other reasons. In addition, FDA may change the type or amount of data provided on this website at any time. Information marked as "Completed" may include measures and/or key projects for which activities are ongoing but no longer tracked as part of FDA-TRACK.