Public Health

What the Trump Administration’s Efforts to Roll Back Federal Regulations Means for Health Programs and Consumer Protections

Amidst a flurry of Executive Orders (EOs) and proclamations, the Trump Administration has also quietlydeclared war on federal regulations, which could hamper the ability of federal agencies—including those that oversee health care programs and consumer protections—to implement, monitor, and enforce federal laws.

Amidst a flurry of Executive Orders (EOs) and proclamations, the Trump Administration has also quietly declared war on federal regulations, which could hamper the ability of federal agencies — including those that oversee health care programs and consumer protections — to implement, monitor, and enforce federal laws.

Regulations interpreting federal statutes are critical for implementation and enforcement of these statutes because they clarify any statutory ambiguities and give regulated entities, such as insurance providers and state Medicaid programs, key details about how to comply with federal law.

Under the federal Administrative Procedures Act (APA), federal agencies must abide by formal rulemaking processes, known as notice and comment, in order to adopt, amend, or repeal binding regulations. However, on April 9, 2025, the Trump Administration issued an EO entitled Directing the Repeal of Unlawful Regulations, which requires agencies to roll back without following the APA’s process for notice and comment existing agency rules that conflict with recent Supreme Court decisions. Read on to learn more about the EO and how it threatens access to healthcare and consumer protections.

Unpacking the Executive Order: Identifying Regulations that Conflict with U.S. Supreme Court decisions

The EO instructs agencies to review all agency regulations, identify any regulations that conflict with a set of 10 recent Supreme Court decisions with administrative law implications, and repeal those regulations. Each of these decisions has been part of a steady erosion of federal agency authority to regulate a wide array of industries, including health care.

It is not immediately clear how agencies will use this list to identify regulations the Trump Administration believes are impacted. Supreme Court decisions are generally written narrowly to address the case at hand, rather than to announce broad new rules. However, Trump Administration officials could try to cite these decisions as justification for repeal of health care regulations adopted under previous administrations on the grounds that the regulations exceeded previous administrations’ authority. Any such attempts would likely result in future litigation.

Regulation Repeal without Notice-and-Comment

After identification of regulations that violate the Supreme Court decisions listed above, the EO directs agencies to repeal these regulations. Typically, to repeal a regulation, agencies must engage in the same notice-and-comment process needed to promulgate rules. However, the EO relies on the APA’s “good cause” exception to direct agencies to bypass notice-and-comment periods, essentially paving the way for mass deregulation with very limited transparency and oversight.

The good cause exception is meant to apply narrowly, when notice and comment is “impracticable, unnecessary, or contrary to the public interest,” and the agency has explained why. Broad use of the APA good cause exception to allow agencies to unilaterally declare broad swaths of regulations illegal without following notice and comment procedure is sure to garner legal challenges, but those challenges will take time.

Meanwhile, the agency regulations and federal oversight of health programs and activities that consumers depend on could be disrupted.

Implications for Health Regulations

Agency review of regulations that may violate the 10 Supreme Court decisions above could have sweeping implications for health-related regulations, including the following:

  • Removal of deference to agency expertise to fill in gaps left in federal statutes could be used to undermine regulations that address novel health care insurance challenges, including those posed by artificial intelligence (AI), new drug development, and health insurance reimbursement complexity. A range of federal health policies, including Medicare and Medicaid coverage decisions, rely heavily on past agency decisions regarding what procedures and forms of care qualify for insurance coverage. Under the EO, HHS may attempt to unilaterally repeal regulations that impose consumer protections on public and private insurance coverage that patients regularly rely on to access care.
  • Regulations that impose a substantial economic impact on industries (including insurers, hospitals, and providers) or that implicate hot-button political issues (such as access to abortion or gender affirming care) may be targeted for repeal.
  • Because of decisions curtailing public health mandates on religious liberty grounds, public health regulations that do not include broad religious exceptions could be at risk.
  • Regulations aimed at improving health equity may be repealed. For example, efforts to improve diversity among the medical provider workforce have already been targeted, and existing programs that target minority health disparities through data collection, funding efforts, and diversified hospital staffing are under threat.

What’s Next?

Efforts to protect public health, improve health equity, and keep health insurance accessible, comprehensible, and affordable are under threat as the Administration pursues aggressive deregulation strategies. There are also likely to be strong legal challenges as the Administration tests the limits of its authority to unilaterally reshape the federal government. Continue to watch this space as CHLPI unpacks these battles and what they mean for health care access and public health.

This article was originally posted by Harvard’s Center for Health Law and Policy Innovation.

About the authors

  • Amy Killelea

    Amy Killelea, J.D. is an assistant research professor at The Georgetown University Center for Health Insurance Reforms.

  • Carmel Shachar

    Carmel Shachar is Health Law and Policy Clinic Faculty Director and Assistant Clinical Professor of Law at Harvard Law School.

  • Elizabeth Kaplan

    Elizabeth Kaplan is director of health care access and a clinical instructor at the Harvard Health Law and Policy Clinic.

  • Mason Barnard

    Mason Barnard is a 3L at Harvard Law School and a concurrent PhD student in Sociology at Princeton University. He researches how the law contributes to the politicization of health and expertise.