by Ariana Del Negro
Editor's Note: The following is the first in a series of articles addressing future regulatory changes for medical devices. In...
Medical Device Regulation: Change is in the Air
As the FDA revamps the medical device approval process, significant overhauls are expected for both the PMA and 510(k) pathways. Medtech Insight is presenting a series of articles focusing on the effect these changes will have to the industry, starting with this first installment focused on potential changes to premarket approvals.