The Food and Drug Administration (FDA) is announcing the following public workshop titled “Streamlining Good Manufacturing Practices (GMPs) for Hearing Aids.” The topic to be discussed is the appropriate level of Good Manufacturing Practices (GMPs) regulation to ensure the safety and effectiveness of air-conduction hearing aid devices.
- Date, Time and Location
- Federal Register Notice
- Webcast
- Registration
- Contact Us
Date, Time and Location
This meeting will beheld April 21, 2016, beginning at 8:30 am – 5:00 pm 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
Webcast
The meeting will be webcast. The webcast link will be available on this web page after April 13, 2016.
If you have never attended a Connect Pro event before, test your connection at https://collaboration.fda.gov/common/help/en/support/meeting_test.htm. To get a quick overview of the Connect Pro program, visit http://www.adobe.com/go/connectpro_overview.
Registration to Attend the Workshop
If you wish to attend this Workshop, you must register by 4:00 pm on April 13, 2016.
There is no fee to register for the Workshop and registration will be on a first-come, first-served basis. Seating is limited so early registration is recommended.
Contact Us
If you require special accommodations due to a disability, 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].
For questions regarding workshop content please contact:
Srinivas Nandkumar, Ph.D., Food and Drug Administration, Center for Devices and Radiological Health, Bldg. 66/Room 2436, 10903 New Hampshire Avenue, Silver Spring, MD 20993, 301-796-6480, FAX:301-847-8126, email: [email protected].