The Food and Drug Administration (FDA) is announcing a public workshop entitled “Medical Device Patient Labeling”. The purpose of the public workshop is to discuss issues associated with the development and use of medical device patient labeling including content, testing, use, access, human factors, emerging media formats, and promotion and advertising. The Center for Devices and Radiological Health is seeking input about these topics from patients and advocacy groups, academic and professional organizations, industry, standards organizations, and governmental agencies.
- Date, Time and Location
- Federal Register Notice
- Agenda
- Registration
- Contact Us
Date, Time and Location
This 2-day workshop will be held September 29-30, 2015, from 8:00 a.m. to 5:00 p.m. each day 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.
Agenda
Preliminary Agenda to be posted shortly.
Registration
If you wish to attend this Workshop, you must register by close of business on September 21, 2015.
Attendance
In-person
Webcast
(1) Name
(2) Title
(3) Affiliation, Company or Organization
(4) E-mail address
(5) Telephone number
(6) Patient Labeling Role [drop down list choices: patient/caregiver; patient educator/advocate; health care provider/facility; manufacturer; labeling developer/writer; distributor/supplier; testing/research; regulation;]
There is no fee to register for the Workshop and registration will be on a first-come, first-served basis. Early registration is recommended because seating is limited.
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].
Contact Us
For questions regarding workshop content please contact:
Antoinette (Tosia) Hazlett, Center for Devices and Radiological Health, Food and Drug Administration, 10903 New Hampshire Avenue, Bldg. 66, Rm 5424, Silver Spring, MD 20993-0002, 301-796-6119, email: [email protected].