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.
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:
6400 Ivy Lane
Greenbelt, MD 20770
The workshop is available by Webcast.
The webcast is available at:
The transcript is available at:
For questions regarding workshop content please contact:
Center for Devices and Radiological Health
Food and Drug Administration
10903 New Hampshire Avenue, WO-66 Room 4110
Silver Spring, MD 20993