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U.S. Department of Health and Human Services

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Percentage of World Trade Organizations (WTO) SPS notifications commented on within 15 days of date assigned

Dictionary: CVM actively participates in the review of animal drug and feed and food related SPS notifications. Notifications are received by the IPT, which then triages the documents and forwards the information on to the respective experts within the center. Typically, the documents are reviewed to determine if proposed SPS standards are consistent with existing international standards, such as CODEX Maximum Residue Limits (MRLs), or that they appear to be appropriate science-based measures to protect human and animal health.

Information is current as of June 30, 2014.

Fiscal Year - 2013

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TimeTargetPercent
Oct 201295100
Nov 201295100
Dec 201295100
Jan 201395100
Feb 201395100
Mar 201395100
Apr 201395100
May 201395100
Jun 201395100
Jul 201395100
Aug 201395100
Sep 201395100

FY 2013 Overall: 100%

Number of WTO SPS notifications commented on (including “No Comment”) within 15 days of receipt during the month

Fiscal Year - 2013
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TimeTargetNumber
Oct 2012N/A4
Nov 2012N/A3
Dec 2012N/A5
Jan 2013N/A5
Feb 2013N/A4
Mar 2013N/A3
Apr 2013N/A5
May 2013N/A7
Jun 2013N/A1
Jul 2013N/A4
Aug 2013N/A12
Sep 2013N/A9

FY 2013 Total: 62

Total number of WTO SPS notifications received during the month

Fiscal Year - 2013
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TimeTargetNumber
Oct 2012N/A4
Nov 2012N/A3
Dec 2012N/A5
Jan 2013N/A5
Feb 2013N/A4
Mar 2013N/A3
Apr 2013N/A5
May 2013N/A7
Jun 2013N/A1
Jul 2013N/A4
Aug 2013N/A12
Sep 2013N/A9

FY 2013 Total: 62

Glossary

SPS

Sanitary and Phytosanitary

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.