lunes, 3 de agosto de 2015

FDA seeks input from the public on "Medical Device Patient Labeling

Information for patients about FDA cardiovascular-related product approvals, safety warnings, notices of upcoming public meetings, and notices about proposed regulatory guidances.

The Center for Devices and Radiological Health (CDRH) is announcing a public workshop on September 29-30, 2015 entitled “Medical Device Patient Labeling”.
The purpose of the 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.
CDRH is especially interested in hearing input from patients and advocacy groups, academic and professional organizations, industry, standards organizations, and governmental agencies.
The upcoming workshop will be held on Tuesday September 29, 2015 and Wednesday September 30, 2015 from 8:00 am to 5:00 pm on both days. The meeting will be held at the FDA White Oak Campus - 10903 New Hampshire Ave, Silver Spring, MD. 20993
If you wish to attend this Workshop, you must register by close of business on September 21, 2015. 
Steve L. Morin
Office of Health and Constituent Affairs
Food and Drug Administration
Helene Clayton-Jeter
Office of Health and Constituent Affairs
Food and Drug Administration
For more information about the Cardiovascular & Endocrine Liaison Program visit the FDA Patient Network

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