FDA Highlights Programs for Innovators at ACR DSI Summit
The FDA joined the ACR®️ Data Science Summit June 9 to give an update about its Total Product Life Cycle Advisory Program.
Read moreThe U.S. Nuclear Regulatory Commission (NRC) published for public comment the regulatory basis corresponding with its long-anticipated, future “Emerging Medical Technologies (EMT)” rulemaking.
The purpose of NRC’s future EMT rulemaking is to establish better pathways into normal NRC regulation for mature EMTs previously regulated via periodically revised guidance. It will likely address uses of strontium-82/rubidium-82 generators, yttrium-90 microsphere brachytherapy and certain radiation therapy EMTs that have matured and are potentially ready for set regulatory requirements.
Public feedback on NRC’s questions will inform future rulemaking. The comment period deadline is Oct. 31.
American College of Radiology® (ACR®) members interested in providing feedback for ACR’s comments can contact Michael Peters, ACR Senior Government Affairs Director. Individuals can also review the regulatory basis and comment on the questions from their own perspectives on Regulations.gov.
FDA Highlights Programs for Innovators at ACR DSI Summit
The FDA joined the ACR®️ Data Science Summit June 9 to give an update about its Total Product Life Cycle Advisory Program.
Read moreLower Fee Now in Effect to File No Surprises Act Disputes
Federal agencies released a final rule that updates the No Surprises Act independent dispute resolution process. The rule lowers the IDR administrative or filing fee from $115 to $15.
Read moreACR Urges Funding for NIH All of Us Program
ACR urges Congress to provide dedicated funding for NIH’s All of Us Research Program, a leader in precision medicine technologies and a valuable tool for researchers.
Read more