FDA Issues Preliminary Report for Postmarket Surveillance
Friday, September 7, 2012
The FDA released a plan this week detailing how it is working to
implement their proposal for improvements to the medical device
postmarket surveillance system.
The plan, "Strengthening Our National System for Medical Device
Postmarket Surveillance," includes strategies the agency is taking to
fully implement the Sentinel System, as well as their suggestions on the
establishment of unique device identifications (UDI) for medical
To read the plan and to submit comments, click here.