To better accommodate data submissions, FDA announced it is deploying enhancements to the Global Unique Device Identification Database (GUDID) and has extended the compliance date to September 24, 2019 for GUDID submission requirements of device constituents of co-packaged combination products assigned to CDER for premarket review.
[membership level=”0,4″][The content continues for paid members only.]
Login or Subscribe [/membership][membership level=”1,5,6,7,8,9,10,11,12″][membership]
