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Number of workshops/conferences for regulatory authorities and industry held in the U.S. in which OIP staff participates during the month
Dictionary: In collaboration with FDA Centers/offices, OIP will participate (e.g. speak, moderate and lead panels) in workshops and conferences for the purpose of improving the technical capacity (e.g. regulations, conducting inspections, enforcement) of regulatory authorities or industry’s knowledge of FDA’s requirements and expectations. This will help ensure that products exported to the U.S. meet FDA requirements.
Fiscal Year - 2010
| Time | Target | Number of Workshops/Conferences |
|---|---|---|
| Oct 2009 | N/A | N/A |
| Nov 2009 | N/A | N/A |
| Dec 2009 | N/A | N/A |
| Jan 2010 | N/A | N/A |
| Feb 2010 | N/A | N/A |
| Mar 2010 | N/A | N/A |
| Apr 2010 | N/A | 15 |
| May 2010 | N/A | 13 |
| Jun 2010 | N/A | 55 |
| Jul 2010 | N/A | 42 |
| Aug 2010 | N/A | 0 |
| Sep 2010 | N/A | 0 |
FY 2010 6-Month Total: 125
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.
