This Act prevents federal agencies from regulating medical practice and restricts interference with a doctor's ability to prescribe FDA-approved drugs for unapproved uses, while preserving existing federal restrictions on certain procedures.
Ron Johnson
Senator
WI
The Right to Treat Act establishes that federal agencies cannot regulate the practice of medicine, reserving that authority for local entities. It specifically prevents federal interference with a doctor's ability to prescribe already-approved drugs for uses not officially sanctioned by the FDA. This Act does not alter existing federal restrictions on procedures like abortion or gender transition interventions.
The Right to Treat Act is a short, sharp piece of legislation that aims to redraw the lines of authority in healthcare. Essentially, it puts federal agencies like the FDA, NIH, and CDC on notice: they are explicitly barred from regulating how doctors practice medicine. This means the federal government can’t step in and tell your physician what medical procedures they can or cannot perform—that authority is pushed down to the state or local level (SEC. 2).
This bill’s most significant move for everyday patients involves drug prescriptions. It protects a doctor’s right to prescribe any FDA-approved drug for a purpose that the FDA hasn't officially sanctioned. This is known as “off-label” use. If a drug is already on the market, a doctor can prescribe it for something else based on their clinical judgment without fear of federal interference (SEC. 2).
For most people, the protection of off-label use is where this bill could make a real difference. Say you have a rare condition, and while there isn't an FDA-approved drug specifically for it, your doctor knows that an existing, approved drug for a different disease has shown promise in trials. Under this Act, your doctor is explicitly shielded from federal rules that might otherwise restrict that prescription. This is a win for physician autonomy and could expand treatment options for patients with complex or uncommon illnesses where standard treatments have failed.
However, this freedom comes with a trade-off: less federal oversight. While federal agencies often standardize care and ensure consistency across state lines, this bill takes that power away. This could mean that standards of care—and the safety checks that go with them—might vary more widely depending on which state you live in, potentially creating a patchwork of medical practice standards.
It’s important to note what this Act doesn’t change. While it pushes back against federal regulation of medical practice generally, it makes very clear that it does not override existing federal laws or policies that restrict specific procedures. The bill explicitly lists abortion, assisted suicide, euthanasia, mercy killing, coercive family planning, female genital mutilation, and gender transition medical interventions as areas where existing federal restrictions remain untouched (SEC. 2).
This creates a politically tailored scope. The Act promotes physician autonomy in areas like drug prescribing while simultaneously ensuring that federal limits on highly sensitive, often debated procedures remain firmly in place. For individuals seeking access to care in those restricted areas, this bill offers no relief and confirms that existing federal barriers will continue to apply. It’s a classic case of giving with one hand while confirming restrictions with the other, making the definition of “Right to Treat” highly selective.