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. 

AMA president Bruce Scott, MD, warns prior authorization is hurting patients and causing doctors to call it quits.

AMA president warns prior authorization hurting patients, driving burnout and practice closures

American Medical Association President Bruce Scott, MD, explains the growing issues with insurance prior authorization impacting patient care and what the AMA is doing about it.

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Cannabis is bad for the heart—should the risk be taken more seriously?

Use of the drug more than doubles a person's risk of dying from heart disease, according to a new analysis of 24 different studies. In a separate editorial, two physicians shared their concerns and highlighted the importance of discussing these risks with patients.

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Radiology societies urge Trump administration to make remote imaging exam supervision permanent

"Eliminating this flexibility would significantly reduce outpatient imaging capacity, forcing many patients to seek services in hospital-based settings," the RBMA contends. 

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Senators introduce bipartisan bill to ban most noncompete clauses

The American College of Emergency Physicians contends the law change would restore physicians’ freedom to choose where they practice and protect their clinical autonomy. 

Veterans Affairs denies it discriminates based on politics, marital status

A report from the Guardian details how the VA removed language protecting patients from discrimination based on political affiliation and lifestyle. The department denies that there has been any actual change in policy.

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Updated: Dexcom recalls more than 700K CGM receivers over safety issues—dozens of adverse events reported

There is an increased risk that these devices will not provide audible alerts for low or high blood glucose levels. The FDA has ruled that this is a Class I recall, highlighting the safety risks associated with missed alerts.

Fed up with patients recording their imaging exams, radiographers call for more stringent cellphone policies

This problem doesn't just affect imaging staff but all healthcare workers, one organization cautions.

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FDA announces recall of interventional product that could cause ‘serious injury or death’

Vendor Centerline Biomedical recently initiated the action, removing certain IOPS (Intra-Operative Positioning System) Guidewires, used in vascular procedures, from the market.