Policy & Regulations

This channel includes news coverage of healthcare policy and regulations set by Congress, the states, Centers for Disease Control and Prevention (CDC), the Department of Health and Human Services (HHS), U.S. Food and Drug Administration (FDA), and medical associations and societies. 

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WHO issues updated brief 'to spark an overdue cultural change in medical imaging'

The new policy brief for healthcare providers stresses the importance of radiation protection and ethically guided care in medical imaging.

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Radiology Partners allegedly conspired with kidney care giant DaVita to stifle competition in labor market

The imaging group has reportedly applied for leniency with the antitrust division, cooperating with the DOJ in exchange for avoiding prosecution. 

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Imaging industry advocate slams feds’ failure to address PET coverage gap in recent ruling

The Society for Nuclear Medicine & Molecular Imaging expressed "strong opposition" following CMS' decision, arguing there is no evidence to support limiting pay for such scans. 

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CMS delays start of Radiation Oncology Alternative Payment Model yet again

The mandatory bundled payment initiative was slated to kick off Jan. 1, 2023, following numerous delays, but will now launch on a to-be-determined date.

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CVS settles opioid case with Florida for $484M

CVS Health has settled with the state of Florida for $484 million to resolve claims for opioid medications filled at CVS pharmacies.

 

 

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Justice Department steps into EHR vendor lawsuit

The U.S. Department of Justice has become involved in a lawsuit against electronic health record (EHR) vendor Modernizing Medicine.

 

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AHA asks Congress to provide more COVID-19 funds

The American Hospital Association (AHA) has asked Congress to provide more financial relief as the COVID-19 pandemic continues.

 

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States move breast cancer screening bills forward

The bills update the ages at which insurance carriers are required to cover screening mammograms and add language that includes tomosynthesis in the definition of mammographic screening.

Around the web

Cardiovascular devices are more likely to be in a Class I recall than any other device type. The FDA's approval process appears to be at least partially responsible, though the agency is working to make some serious changes. We spoke to a researcher who has been tracking these data for years to learn more. 

Updated compensation data includes good news for multiple subspecialties. The new report also examines private equity's impact on employment models and how much male cardiologists earn compared to females.

When drugs are on the FDA’s shortage list, outsourcing facilities can produce their own compounded versions. When the FDA removed tirzepatide from that list with no warning, it created a considerable amount of chaos both behind the scenes and in pharmacies all over the country. 

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