About FDA
Total number of RFDs filed by OCP in the month
Dictionary: The Office of Combination Products (OCP) is responsible for classifying products as either drugs, devices, biologics, or combination products and to assign the product to a Center for regulation. By submitting a RFD, a company may obtain a formal FDA determination of the status of their product. OCP must respond to a RFD within 60 days, or the requestor's recommended classification stands. A proper determination by OCP will enable the Agency to assign a particular product to the appropriate agency component for premarket review and postmarket regulation (CDER, CBER, or CDRH), and also enable the Agency to regulate the product under the proper regulatory authorities (NDA, 510(k), PMA, or BLA).
Information is current as of December 31, 2012.
Fiscal Year - 2011
| Time | Target | Number of RFDs |
|---|---|---|
| Oct 2010 | N/A | 5 |
| Nov 2010 | N/A | 3 |
| Dec 2010 | N/A | 1 |
| Jan 2011 | N/A | 2 |
| Feb 2011 | N/A | 6 |
| Mar 2011 | N/A | 2 |
| Apr 2011 | N/A | 3 |
| May 2011 | N/A | 3 |
| Jun 2011 | N/A | 8 |
| Jul 2011 | N/A | 5 |
| Aug 2011 | N/A | 3 |
| Sep 2011 | N/A | 2 |
FY 2011 Total: 43
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.
