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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 June 30, 2014.

Fiscal Year - 2012

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TimeTargetPercentage
Oct-Dec 20119098
Jan-Mar 20129094
Apr-Jun 20129093
Jul-Sep 20129094

FY 2012 Overall: 95%

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

Fiscal Year - 2012
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TimeTargetNumber
Oct-Dec 2011N/A92
Jan-Mar 2012N/A84
Apr-Jun 2012N/A108
Jul-Sep 2012N/A82

FY 2012 Total: 366

Total number of analytical packages reviewed within CMS in the quarter

Fiscal Year - 2012
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TimeTargetNumber
Oct-Dec 2011N/A94
Jan-Mar 2012N/A89
Apr-Jun 2012N/A116
Jul-Sep 2012N/A87

FY 2012 Total: 386

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.