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.
Update On and Look Ahead At FDA’s Changes to the 510(k) Process brings together Representatives of marketers and manufacturers of 510(k) medical devices, including outside FDA counsel, in-house counsel, regulatory consultants and regulatory affairs personnel.
