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The approval, made as part of a special FDA pilot program, took just 50 days.

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An interventional cardiologist believes he was targeted and terminated for being outspoken about a series of incidents at his hospital. 

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The cardiovascular care of thousands of Missouri patients is suddenly up in the air. The heart of the issue is a practice's alleged interest in opening up a new private equity-backed clinic.  

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In particular, rads working in breast imaging and pediatrics appear to notch the lowest rates of career advancement, experts write in Current Problems in Diagnostic Radiology

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David M. Cutler, PhD, a noted researcher and professor, shared his thoughts on the specialty in an editorial published by JAMA Health Forum

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Lancaster Radiology Associates and Penn Medicine had together owned both the MRI Group and PET Partnership, operating six centers in the Keystone State. 

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Ohio Senate Bill 324 would exempt NPs and PAs from certain licensure requirements, allowing them to supervise X-ray machine operators. 

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True Definition DL was designed to help produce detailed, high resolution images without protocol or workflow adjustments.

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These actions represent "a significant threat to the integrity of radiology research," authors of a new analysis caution.

Part of the ASNC delegation that visited with congressional members to to explain policy and payment challenges that face. Members of ASNC's Health Policy Committee from left: Daniel Huck, MD, MPH, David E. Winchester, MD, MS, FASNC, Suman Tandon, MD, FASNC, Vikas Veeranna, MD, Friederike Keating, MD, FASNC, and Attila Feher, MD, PhD.

The American Society of Nuclear Cardiology made its voice heard, pushing for legislation to repeal Medicare payment cuts and tie payments to inflationary increases. Prior authorization and a proposed tariff on radioisotopes were also discussed.

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A bad outcome for Johnson & Johnson MedTech just got worse. A jury previously ordered the company to pay $147M, but the new total is $442M.

Artificial intelligence could serve as an effective tool for determining which patients may need additional breast MRI sequences mid-protocol.

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The approval, made as part of a special FDA pilot program, took just 50 days.