Regulatory & PolicySTAT’s recent investigation uncovers key details about Nutex Health’s use of the No Surprises Act to engineer a dramatic financial turnaround. This analysis explores regulatory nuances, Nutex’s evolving business model, and the wider implications for America’s micro hospital and emergency room landscape.
Dr. Alex Morgan·Jun 29, 2026
Medical TechnologyHealthcare data lakes were once seen as the future for storing vast volumes of information, promising analytic breakthroughs for research and patient care. Increasingly, stakeholders warn these lakes are turning into 'swamps,' hampered by unusable data, challenging navigation, and uncertainty on what value can really be extracted. We take an independent look at why these problems have emerged, how they impact care delivery and health system operations, and strategies being developed to turn swamps back to lakes.
Dr. Alex Morgan·Jun 27, 2026
Regulatory & PolicyUnder President Trump, moves to consolidate scientific leadership and oversight within the CDC have sparked renewed debate over the agency’s independence from political influence. This article explores who stands to gain or lose from the restructuring, the context of CDC’s evolving role, and broader implications for the credibility of federal health agencies.
Dr. Alex Morgan·Jun 25, 2026
Biopharmaceutical IndustryAs U.S. employers grapple with the rising cost of healthcare, Priority Health’s new collaboration with Garner Health seeks to address these challenges head-on by steering plan members toward high-quality physicians. The move is designed to optimize patient outcomes while realizing tangible savings for both employers and employees.
Dr. Alex Morgan·Jun 25, 2026
Biotech InnovationThe experimental psychedelic ibogaine has drawn significant attention as an unapproved treatment for substance use disorder (SUD). While many clinicians remain skeptical of its efficacy and safety, they nevertheless face new responsibilities as some patients pursue this unconventional route. Examining ibogaine's signal, risk profile, and the evolving role of providers in the changing landscape of SUD care.
Dr. Alex Morgan·Jun 24, 2026
Medical TechnologyAs OpenEvidence prepares to integrate a newly FDA-cleared AI tool into its platform for heart disease detection, the intersection of machine learning and cardiovascular healthcare takes a significant leap forward. This development draws attention not only for its clinical applications, but also for the broader context of how regulated artificial intelligence is reshaping treatment paradigms and approaches to chronic disease worldwide.
Dr. Alex Morgan·Jun 23, 2026
AI in Drug DiscoveryThe increasing integration of AI in clinical settings has ignited debate about the presence of bias in these tools. While some argue for bias-free models, others contend that AI must recognize and account for real-world disparities to improve care delivery and outcomes.
Dr. Alex Morgan·Jun 21, 2026
Biopharmaceutical IndustrySTAT News recently showcased a wide array of reader opinions, particularly focusing on blue zones and open-access publishing fees. These debates shed light on the complex, sometimes contentious, intersections of public health knowledge, research communication, and the incentive structures in modern science. The diversity and depth of views shared by readers reveal enduring disagreements and evolving priorities in biomedicine.
Dr. Alex Morgan·Jun 20, 2026
Medical TechnologyA major debate has emerged around the value and safety of elective whole-body MRI services promoted to healthy adults. Two leading radiologists, writing in a JAMA editorial, have taken aim at the marketing claims of several companies, suggesting that such scans could trigger more medical harm than benefit. The industry’s three largest firms have pushed back on those criticisms, defending the utility of their offerings.
Dr. Alex Morgan·Jun 18, 2026
Regulatory & PolicyA high-stakes lawsuit from the Federal Trade Commission and four state attorneys general targets a prominent transgender health professional body’s care standards. The legal maneuver signals profound questions about regulatory boundaries and medical best practices in the era of politicized healthcare.
Dr. Alex Morgan·Jun 17, 2026
Biotech InnovationThe termination of Be Biopharma’s hemophilia B cell therapy trial underscores the persistent scientific and commercial challenges in advancing novel therapies for hemophilia. This development adds to a growing list of recent withdrawals in the field and raises broader questions for biotech companies and investors navigating unmet needs and competitive dynamics in rare disease drug development.
Dr. Alex Morgan·Jun 17, 2026
Biopharmaceutical IndustrySupplement use in the United States has not remained static. From vitamin C frenzy to the mainstreaming of protein powders and probiotics, each decade has delivered new motivations and products for consumers. This piece traces the evolution, the forces involved, and potential implications for medicine and wellness.
Dr. Alex Morgan·Jun 16, 2026