The U.S. Food and Drug Administration FDA announced that the agency is formally asking for submissions on how to improve existing regulations. FDA expects that retrospective reviews like this would help FDA focus on how to improve regulations.
Where are regulations ineffective?
Do regulations address current public health challenges?
Is there a need to update regulations?
Can regulations be revised in ways that make them less burdensome without making them less effective?
Are there regulatory requirements that are redundant, inconsistent or needlessly overlap?