Health knowledge made personal
Join this community!
› Share page:
Go
Search posts:

Draft Guidance for Industry and Food and Drug Administration Staff - eCopy Program for Medical Device Submissions

Posted Oct 16 2012 12:00am
The purpose of this guidance is to explain the new electronic copy (eCopy) Program for medical device submissions. At this time, submission of an eCopy of a medical device submission is voluntary. However, section 745A(b) of the Federal Food, Drug, and...
Post a comment
Write a comment:

Related Searches