About FDA
Percentage of NDI notification reviews completed to which FDA objected
Dictionary: Timely review of notifications of new dietary ingredients impacts the public health by preventing substances that are not actually dietary ingredients from being used in dietary supplements, and assuring that new dietary ingredients have adequate evidence for presumption of safety. Since these statutory requirements are notifications rather than pre-market approvals, it is essential that ONLDS have completed review of the information before the submitter markets the product, to notify them of any safety or regulatory concerns before the product reaches consumers.
Information is current as of December 31, 2012.
Fiscal Year - 2011
| Time | Target | Percentage |
|---|---|---|
| Oct 2010 | N/A | 80 |
| Nov 2010 | N/A | 100 |
| Dec 2010 | N/A | 67 |
| Jan 2011 | N/A | 75 |
| Feb 2011 | N/A | 75 |
| Mar 2011 | N/A | 67 |
| Apr 2011 | N/A | 87 |
| May 2011 | N/A | 0 |
| Jun 2011 | N/A | 67 |
| Jul 2011 | N/A | 50 |
| Aug 2011 | N/A | 100 |
| Sep 2011 | N/A | 75 |
FY 2011 Overall: 70%
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.
