ACR is asking the imaging community to contact their federal representatives, urging them to pass three key pieces of legislation before Jan. 1. 

The lawsuit names Betty Matthew, MD, Advanced Radiology Consultants and Hartford HealthCare, both in Connecticut, as defendants. 

The VA is throwing in with the FDA to launch a cross-agency AI testing facility. 

As debate simmers over how best to regulate AI, experts continue to offer guidance on where to start, how to proceed and what to emphasize. A new resource models its recommendations on what its authors call the “SETO Loop.”

Oral decongestants containing phenylephrine were found not to be effective. However, nasal sprays of the same drug are not subject to the FDA’s proposed order.

Samantha Maltin, a former marketing executive at Sesame Workshop, will now lead branding and public outreach initiatives at St. Jude Children's Research Hospital. 

Given the complex nature of intrahepatic cholangiocarcinoma, efforts to develop more effective methods of treating it have increased over the years.

Johnson & Johnson is now the third company with an FDA-approved PFA system in its portfolio, joining Medtronic and Boston Scientific. Varipulse previously gained CE mark approval in February. 

FDA Commissioner Robert Califf, MD, said the clinical community needs to combat health misinformation at a grassroots level. He warned that patients are immersed in a "sea of misinformation without a compass."

Free-text reporting also was associated with significant omissions in abdominal anatomical structures, researchers detailed in the journal Cureus.