Update On and Look Ahead At FDA’s Changes to the 510(k) Process 2012

Update On and Look Ahead At FDA’s Changes to the 510(k) Process is a webinar dedicated to the background behind FDA’s decision to modify the 510(k) process, outline the progress it has made in 2011and 2012 to implement these changes, and take a look at what changes are yet to come in 2012 and beyond.

Who should Attend

Representatives of marketers and manufacturers of 510(k) medical devices, including outside FDA counsel, in-house counsel, regulatory consultants and regulatory affairs personnel.