Device Makers Identify More FDA Regulations Worth Revising
This article was originally published in The Gray Sheet
Executive Summary
Device makers have proposed several regulations that FDA should revisit to lighten manufacturers' burdens as part of the agency's ongoing regulatory review.
You may also be interested in...
Less Equipment Would Be Stocked At Ambulatory Surgical Centers Under CMS Proposal
A government plan to slash regulatory burdens for health care providers would, among other changes, reduce the amount and type of emergency medical equipment required at ambulatory surgical centers.
Less Equipment Would Be Stocked At Ambulatory Surgical Centers Under CMS Proposal
A government plan to slash regulatory burdens for health care providers would, among other changes, reduce the amount and type of emergency medical equipment required at ambulatory surgical centers.
Agencies Launch White House-Mandated Review Of Regulations
FDA and CMS announced preliminary plans May 26 for updating, streamlining or eliminating certain regulations in response to a White House request.