For over three decades, CEI has advocated health care reforms that put more power in the hands of consumers to choose their health providers, treatment protocols, and scope of insurance coverage. We have advocated reform of the Food and Drug Administration’s drug and device approval process to allow for greater flexibility and patient choice. And in 2013, CEI organized the court challenges to Obamacare’s exchange subsidies that concluded with the Supreme Court’s King v. Burwell decision.
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Featured Posts

News Release
Senate Parliamentarian Eliminates Medicaid Reform Provisions, Leaving Costs/Problems Intact
The Senate’s parliamentarian has determined that many of the Medicaid provisions in the One Big Beautiful Bill cannot be passed with simple majority vote via…

Blog
FDA can’t stomach fluoride and doesn’t want you to, either
On May 13, the Food and Drug Administration (FDA) announced that it would begin a process intended to exclude ingestible prescription fluoride products for…

Blog
Free the Economy podcast: Drug costs and benefits with Sally Pipes
In this week’s episode we cover reforms to the Endangered Species Act, attacks on US tech firms, nuclear power innovation,…
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National Review
Cancel Culture Comes to Medicine
Cancel culture has come to medicine. Dr. Scott Atlas, who was chairman of neuroradiology at Stanford’s medical school until 2012 and more recently a senior fellow…
News Release
Report: Politics, Not Science, Drives Double Standard on Cannabis, Nicotine Policies
As the House votes on a bill this month to end the federal prohibition on cannabis – once unthinkable – a new Competitive Enterprise…
Blog
Trump’s Drug Price Controls are a Lousy Deal for Patients
Prescription drug prices are popular targets for lawmakers—especially in an election year. Still, it came as quite a surprise when President Trump issued an…
The Washington Examiner
Government Alcohol Advice Should be Based on Evidence, Not Agendas
Should adults cut their alcohol consumption in half for health reasons? That’s what a federal government advisory committee is recommending. It matters because that recommendation…
Blog
FDA Rules on E-cigarette Makers Go into Effect Today, to the Detriment of Public Health
The world was simpler in 2009 when Congress enacted a law that gave the Food and Drug Administration (FDA) the power to regulate tobacco. Back…
The Hill
Ending Counterproductive, Counterintuitive Regulation
Early in the COVID-19 crisis, House Speaker Nancy Pelosi (D-Calif.) chided the Trump administration’s response and demanded “testing, testing, testing.” Yet, when…