Medical Devices
Public Workshop - Leveraging Registries With Medical Device Data for Postmarket Surveillance and Evidence Appraisal Throughout the Total Product Life Cycle, September 12-13, 2012
The Food and Drug Administration (FDA) is announcing a public workshop entitled: Leveraging Registries with Medical Device Data for Postmarket Surveillance and Evidence Appraisal Throughout the Total Product Life Cycle.” The topic to be discussed is best practices for use of registries with medical device data for postmarket surveillance, clinical studies, and evidence appraisal.
Date, Time and Location
This workshop was held September 12, 2012, from 8:00 a.m. to 5:00 p.m. and September 13, 2012, from 8:00 a.m. to 5:00 p.m., at the following location:
Greenbelt Marriott
6400 Ivy Lane
Greenbelt, MD 20770
301-614-8202
The workshop is available by Webcast.
Webcast
The webcast is available at:
Contact Us
For questions regarding workshop content please contact:
Danica Marinac-Dabic
Center for Devices and Radiological Health
Food and Drug Administration
10903 New Hampshire Avenue, WO-66 Room 4110
Silver Spring, MD 20993
301-796-6689
email: Danica.Marinac-Dabic@fda.hhs.gov
