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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CHIME: Streamline MU, add flexibility

Meaningful Use (MU) needs streamlining and a reduced reporting burden for provider through better aligned quality measures, said the College of Healthcare Information Management Executives (CHIME). 

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Coder productivity down in wake of ICD-10 transition

As critics predicted, the ICD-10 transition is negatively impacting inpatient and outpatient coder productivity at hospitals of all sizes and types.

Health system announces new plan to refund patients if expectations aren't met

The Pennsylvania-based Geisinger Health System has unveiled its ProvenExperience program, which offers refunds to patients who don’t have their expectations met while receiving care. 

Healthcare leaders spanning the globe urge U.S. presidential hopefuls to back openness on clinical trials

Close to 60 physicians, medical researchers and public-health experts from around the world are imploring American presidential candidates to state whether they support access to all clinical trial data held by U.S. federal agencies—regardless of the trials’ topics, findings, sponsors or geographical settings. 

Lumenis Acquires Israeli-Based Pollogen Strengthening and Expanding Its Aesthetic Division

Lumenis Ltd., the world's largest energy-based medical device company for aesthetic, surgical and ophthalmic applications, announced today that the company has completed the acquisition of Pollogen Ltd. 

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CMS reports smooth ICD-10 transition to date

The transition to ICD-10 is going well, according to the first numbers released by the Centers for Medicare & Medicaid Services. 

Senators introduce bipartisan bills to expedite FDA approval for medical devices

Republican senator Cory Gardner (Colorado) and Democrat senator Joe Donnelly (Indiana) introduced two bills on Oct. 21 to accelerate the FDA approval process for medical devices.

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The transition finally happens

After years of debate, several delays and lots of preparation, the big news this week was that it's finally time to start using the ICD-10 codeset. 

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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