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U.S. Department of Health and Human Services

About FDA

Percentage of analytical package reviews received via FDA's electronic Compliance Management System (CMS) that meet Office of Compliance (OC) timeframes as specified in CMS in the quarter

Dictionary: FDA ensures the safety of regulated products in part by performing laboratory analyses that monitor compliance with its regulations. If foods, dietary supplements or cosmetics are found to contain potentially unsafe contaminants during FDA laboratory analyses then the analytical packages must be reviewed to determine if they support regulatory action. Improving the efficiency of analytical regulatory package reviews will speed enforcement actions and more rapidly ensure the safety of U.S. foods, dietary supplements and cosmetics by removing potentially harmful products from the marketplace.

Information is current as of March 31, 2014.

Fiscal Year - 2014

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TimeTargetPercentage
Oct-Dec 20139099
Jan-Mar 20149097
Apr-Jun 201490TBD
Jul-Sep 201490TBD

FY 2014 YTD: 98%

Number of analytical package reviews received via CMS that meet OC timeframes in the quarter

Fiscal Year - 2014
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TimeTargetNumber
Oct-Dec 2013N/A69
Jan-Mar 2014N/A60
Apr-Jun 2014N/ATBD
Jul-Sep 2014N/ATBD

FY 2014 YTD: 129

Total number of analytical packages reviewed within CMS in the quarter

Fiscal Year - 2014
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TimeTargetNumber
Oct-Dec 2013N/A70
Jan-Mar 2014N/A62
Apr-Jun 2014N/ATBD
Jul-Sep 2014N/ATBD

FY 2014 YTD: 132

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.