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U.S. Department of Health and Human Services

About FDA

Percent of eRadHealth submissions submitted electronically during the month

Dictionary: One of OIR's functions is to monitor devices that emit radiation. OIR has developed a database which collects information about radiation emitting devices. eRadHealth allows manufacturers to submit radiation documentation in electronic format so that FDA can provide risk management prioritization of data, provide trend analyses, and allow data sharing with states and the public. Electronic information is essential to providing accessible information therefore permitting efficient use of FDA resources and expediting industry-wide corrections of product safety problems.

Information is current as of September 30, 2013

Fiscal Year - 2010

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TimeTargetPercent
Oct 20091510
Nov 2009159
Dec 20091518
Jan 20101512
Feb 20101510
Mar 20101510
Apr 20101513
May 20101511
Jun 2010158
Jul 20101516
Aug 20101516
Sep 20101515

FY 2010 Overall: 13%

Number of eRadHealth electronic submissions submitted during the month

Fiscal Year - 2010
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TimeTargetNumber
Oct 2009N/A38
Nov 2009N/A31
Dec 2009N/A54
Jan 2010N/A30
Feb 2010N/A23
Mar 2010N/A34
Apr 2010N/A39
May 2010N/A31
Jun 2010N/A29
Jul 2010N/A60
Aug 2010N/A110
Sep 2010N/A110

FY 2010 Total: 589

Total number of eRadHealth submissions (electronic and paper) submitted during the month

Fiscal Year - 2010
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TimeTargetNumber
Oct 2009N/A387
Nov 2009N/A346
Dec 2009N/A294
Jan 2010N/A246
Feb 2010N/A225
Mar 2010N/A348
Apr 2010N/A310
May 2010N/A274
Jun 2010N/A362
Jul 2010N/A384
Aug 2010N/A704
Sep 2010N/A713

FY 2010 Total: 4,593

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.