HR 4132

0likes☆Favorite🔕SubscribeShare

Introduced ↻ Update bill dataRe-checks Congress.gov for new actions and updates the bill's status, and fills in any sponsors, committees, or related bills that are missing. It does not re-pull sponsors/cosponsors/committees/related — those rarely change — and it skips all work if nothing has changed upstream, so it's cheap to click. Contact your reps Urge the sponsor

IN THE HOUSE OF REPRESENTATIVES

June 25, 2025

Mrs. Harshbarger (for herself, Ms. Sherrill, Mr. Valadao, Mr. Davis of North Carolina, Mr. Calvert, Ms. Ross, Ms. Letlow, Mr. Peters, Mr. Schneider, Mr. Womack, and Mr. Tonko) introduced the following bill; which was referred to the Committee on Energy and Commerce

A BILL

To provide for digital communication of prescribing information for drugs (including biological products), and for other purposes.

Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,

SECTION 1. SHORT TITLE.

This Act may be cited as the “Prescription Information Modernization Act of 2025”.

SEC. 2. DIGITAL COMMUNICATION OF FDA-APPROVED PRESCRIBING INFORMATION FOR DRUGS (INCLUDING BIOLOGICAL PRODUCTS).

(a) In General.—Section 502(f) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 352(f)) is amended by adding at the end the following: “Required prescribing information for drugs subject to section 503(b)(1) may be made available solely by electronic means provided that the labeling complies with all applicable requirements of law, that the manufacturer affords prescribers and dispensers the opportunity to elect to also continue to receive all such information in paper form, or to request paper labeling on an as-needed basis, and after such request, and that the manufacturer promptly provides the requested information without additional cost.”.

(b) Rulemaking.—

(1) In general.—Not later than 1 year after the date of the enactment of this Act, the Secretary of Health and Human Services shall issue final regulations to—

(A) implement the amendment made by subsection (a); and

(B) provide instructions on how health care professionals can receive paper copies of prescribing information directly from the manufacturer or distributor if desired.

(2) Economic impacts.—The Secretary of Health and Human Services shall design the regulations required by paragraph (1) so as to minimize the adverse economic impacts of such regulations on prescribers and dispensers.

(c) Public Workshop.—Not later than 2 years after the date of the enactment of this Act, the Secretary of Health and Human Services, acting through the Commissioner of Food and Drugs, shall hold a public workshop with relevant stakeholders to discuss how to continue to optimize the format, accessibility, and usability of prescribing information.

(d) Effective Date.—The amendment made by subsection (a) shall apply with respect to drugs introduced or delivered for introduction into interstate commerce on or after the sooner of—

(1) the date that is 2 years after the date of the enactment of this Act; or

(2) the effective date of the final regulations promulgated to implement such amendment.

(e) Definition.—In this section, the term “drug” has the meaning given to such term in section 201 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321). <all>