Next month the Food and Drug Administration (FDA) will hold a public workshop on “Medical Device Patient Labeling.” According to the Federal Register, the purpose 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.” (pp. 43093-43094)
The two-day event will be September 29th and 30th at the FDA White Oak Campus in Silver Spring Maryland. For those that can’t attend in person, a webcast will be available.