‘We Need More Time‘: Medtech Groups Testify Before EPA On ETO Emissions Regulation
Medtech groups call for extended commentary and compliance periods for two new EtO regulations from the EPA.
You may also be interested in...
CDRH is on track to meet its MDUFA V goals, seeing a steady return to pre-pandemic levels of device authorizations and submissions.
The EPA and medtech industry want the same things: Cleaner air and a steady supply of medical devices. So how do they reconcile their differences?
The deadline for comments on the Environmental Protection Agency proposal, which trade groups say could lead to device shortages if implemented, has been moved from 12 June to 27 June.