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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 - 2011

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TimeTargetPercent
Oct 20101514
Nov 20101514
Dec 20101519
Jan 20111528
Feb 20111515
Mar 20111521
Apr 20111517
May 20111512
Jun 20111523
Jul 20111512
Aug 20111515
Sep 20111532

FY 2011 Overall: 19%

Number of eRadHealth electronic submissions submitted during the month

Fiscal Year - 2011
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TimeTargetNumber
Oct 2010N/A49
Nov 2010N/A42
Dec 2010N/A61
Jan 2011N/A76
Feb 2011N/A41
Mar 2011N/A73
Apr 2011N/A58
May 2011N/A38
Jun 2011N/A77
Jul 2011N/A43
Aug 2011N/A117
Sep 2011N/A217

FY 2011 Total: 892

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

Fiscal Year - 2011
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TimeTargetNumber
Oct 2010N/A343
Nov 2010N/A296
Dec 2010N/A318
Jan 2011N/A267
Feb 2011N/A270
Mar 2011N/A343
Apr 2011N/A333
May 2011N/A305
Jun 2011N/A336
Jul 2011N/A368
Aug 2011N/A765
Sep 2011N/A673

FY 2011 Total: 4,617

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.