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CMS and the FDA say the goal is to improve patient access to medical devices that address an unmet need.

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“Radiologists should exercise caution when implementing...protocoling workflows that bypass independent radiologist review," one expert writes in the American Journal of Roentgenology

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Co-founders Jonathan Steinberger, MD, and Gabriel Lipshutz, MD, are starting Elmnt IR with an initial location in Los Angeles and more to follow.  

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About 39% of rads polled by the news website said they fall in this income bracket, placing the profession in a tie with orthopedists. 

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Members of the specialty are more likely to trust domain-specific models when it comes to report generation support, research suggests. 

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The largest single component of the overall project is likely to be the high-tech, high-touch hospital that’s now slated for opening in 2030.

The U.S. Department of Justice said Wisconsin-based Apple Clinic and its owner Michael Johnson, MD, were using a combination of nerve density testing, vitamin injections and electrical stimulation to alleviate pain, billing Medicare for these medically unnecessary services. 

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Post-thrombotic syndrome is the result of permanent damage to the veins following DVT. The condition causes swelling, discoloration and pain in the legs and can feel debilitating for many.

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Medmo and Covera Health, both based in New York, officially announced their merger on April 21, with the latter’s lead investor, Insight Partners, funding the deal. 

The companies say they’re entering the next phase of collaboration, offering GEHC mammography systems paired with AI offerings from DeepHealth. 

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Speaking at a Politico health care policy forum, CMS Administrator Mehmet Oz, MD, said he supports Medicaid, adding that “when you love something, you protect it.”

The insurance giant has been piloting a program to speed up reimbursement to hospitals in 10 states, reducing delays by roughly 50%. Now, the company said it will work to lift prior authorization barriers on patient care delivery. The intent is to roll out these changes nationwide by the end of 2026, UnitedHealthcare confirmed.

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CMS and the FDA say the goal is to improve patient access to medical devices that address an unmet need.