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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 February 28, 2013.

Fiscal Year - 2013

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TimeFiscal Year TargetPercent
Oct 201295100
Nov 201295100
Dec 201295100
Jan 201395100
Feb 201395100
Mar 201395TBD
Apr 201395TBD
May 201395TBD
Jun 201395TBD
Jul 201395TBD
Aug 201395TBD
Sep 201395TBD

FY 2013 YTD: 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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TimeFiscal Year TargetNumber
Oct 2012N/A4
Nov 2012N/A3
Dec 2012N/A5
Jan 2013N/A5
Feb 2013N/A4
Mar 2013N/ATBD
Apr 2013N/ATBD
May 2013N/ATBD
Jun 2013N/ATBD
Jul 2013N/ATBD
Aug 2013N/ATBD
Sep 2013N/ATBD

FY 2013 YTD: 21

Total number of WTO SPS notifications received during the month

Fiscal Year - 2013
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TimeFiscal Year TargetNumber
Oct 2012N/A4
Nov 2012N/A3
Dec 2012N/A5
Jan 2013N/A5
Feb 2013N/A4
Mar 2013N/ATBD
Apr 2013N/ATBD
May 2013N/ATBD
Jun 2013N/ATBD
Jul 2013N/ATBD
Aug 2013N/ATBD
Sep 2013N/ATBD

FY 2013 YTD: 21

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.