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Abortion Advocates Brace For Impact As SCOTUS EMTALA Case Looms

Women’s rights advocates, providers and other stakeholders are raising concerns that the consolidated pair of impending Supreme Court cases up for oral arguments Wednesday (April 24) could have dire consequences for emergency medical protections and access to stabilizing treatment.

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A report co-sponsored by FDA suggests many clinical trial sponsors want the agency’s help on how to comply with the reporting requirements for HHS’ clinical trials database, Clinicaltrials.gov -- a database suffering from significant gaps and over which FDA has enforcement responsibility.

FDA's Regan-Udall Foundation and the ASH Research Collaborative (ASH RC) are launching a collaborative project to gather real-world evidence for sickle cell disease, aiming to establish a consensus on using electronic health record data to better understand clinical outcomes among sickle cell patients and broaden research in the field.

Implementing site-neutral Medicare payment policies could replace the budget neutrality requirements that have driven cuts to physician pay while supporting independent practices and lowering overall health care costs for the American people,

The top Republican on the Senate health committee is criticizing FDA’s approach to regulating clinical decision support (CDS) software, asking the agency for more information about how it crafted its guidance on the technology and whether it has documentation of threats posed to patients.

State insurance regulators have established a multi-state steering group that will look at how February’s cyberattack on Change Healthcare unfolded, assess how insurance carriers and other impacted entities reacted, and facilitate discussions about the response and recovery efforts with UnitedHealth Group and Change Healthcare, as well as ensure the country is better prepared for the next, inevitable attack.