The Food and Drug Administration (FDA) is announcing a public workshop entitled “Medical Device Patient Labeling”. The purpose of the public workshop was 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
- Webcast Archive
- Agenda
- Contact Us
Date, Time and Location
This 2-day workshop was 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
Webcast Archive
- September 29th
- September 30th
Introduction
Day 1 – Morning Part I
Day 1 – Morning Part II
Day 1 – Afternoon
Day 2
Agenda
Day 1, September 29, 2015
Day 2, September 30, 2015
[email protected].