Healthcare DIVE July 15, 2024
Nick Paul Taylor

Lawmakers said the final rule carries “the risk of greatly altering the United States’ laboratory testing infrastructure.”

Lawmakers have told the Food and Drug Administration to suspend efforts to implement its final rule on laboratory developed tests (LDTs).

The House Appropriations Committee made the request Wednesday in legislation about funding the FDA and other federal agencies will receive in its 2025 financial year. Committee members backed the appropriations bill by a 29-26 vote.

As well as agreeing to provide the FDA with $3.5 billion in direct appropriations, the lawmakers shared advice on how the agency should use the money. The recommendations include a call to suspend work on the final rule and partner with Congress to modernize the regulation...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: Congress / White House, FDA, Govt Agencies, Provider
Seniors deserve timely access to care, not bureaucratic hurdles | Viewpoint
Trump names nominees to lead CDC, FDA, and his pick for surgeon general
Trump Nominates Physicians for CDC Director, Surgeon General
Rand roadblock: Biotech bill’s uncertain future
Advocate Health takes to Capitol Hill on hospital at home: 5 notes

Share This Article