The Food and Drug Administration (FDA) is announcing a public meeting on the reauthorization of the medical device user fee program. The current legislative authority for the medical device user fee program expires in September 2017 and new legislation will be required for FDA to continue collecting user fees for the medical device program.
- Date, Time and Location
- Federal Register Notice
- Agenda
- Registration
- Contact Us
Date, Time and Location
This meeting will be held on Monday, July 13, 2015, from 9:00 a.m. – 5:00 p.m. at the following location:
FDA White Oak Campus
10903 New Hampshire Avenue
Bldg. 31, Room 1503 (the Great Room)
Silver Spring, MD, 20993
- FDA Campus Information (Airports, Directions, Lodging Accommodations, Public Transportation, etc.)
The meeting will be webcast. More information about the webcast (including the link) will be posted here by Monday, July 6, 2015.
Agenda
Registration
If you wish to attend this meeting or view the webcast, you must register by close of business on July 2, 2015.
There is no fee to register for the meeting and registration will be on a first-come, first-served basis. Early registration is recommended because seating is limited.
If you wish to make an oral presentation during any of the open comment sessions at the meeting you must indicate this at the time of registration. FDA requests that presentations focus on the areas defined in the Federal Register Notice. You should also identify which discussion topic(s) you wish to address in your presentation. FDA will do its best to accommodate requests to speak.
If you require special accommodations, or need additional information regarding registration, please contact Susan Monahan, Office of Communication and Education, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, Bldg. 32, Silver Spring, MD 20993, 301-796-5661, [email protected].
Contact Us
For questions regarding meeting content please contact:
Aaron Josephson, Center for Devices and Radiological Health, Food and Drug Administration, Building 66, Room 5449, 10903 New Hampshire Ave., Silver Spring, MD 20993, 301-796-5178 [email protected]