The legislation, the “Food and Drug Administration Safety and Innovation Act,” was written to reauthorize the FDA’s prescription drug user fee program, which allows the FDA to collect fees from drug manufacturers to support the agency’s operations.
Title X of the bill includes provisions to help prevent drug shortages, including a requirement that manufacturers notify the FDA when the production of certain drugs would be interrupted and a requirement that the Drug Enforcement Administration provides timely updates on drug quota increases to manufacturers.
The U.S. Senate will vote on the legislation this week, and the president is expected to sign the bill into law soon afterwards.
Related Articles on Anesthesia:
What Does Medicare’s 3-Day Payment Rule Mean for Anesthesia and Pain Practices?
Anesthesiologist to Serve Sixth Consecutive Term on AMA Board
University of Alabama Appoints Anesthesiology Professor Emeritus
At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.
