The FDA announced that it will be holding a public 2-day workshop on September 29-30, 2015, from 8:00 a.m. to 5:00 p.m. titled, “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.
For more information on the location, agenda and how to register, please click here.
