H.R. 1931

119 HR 1931 IH: Access to Pediatric Technologies Act of 2025
 U.S. House of Representatives
 2025-03-06
 text/xml
 EN
 Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain.
 I  119th CONGRESS  1st Session  H. R. 1931  IN THE HOUSE OF REPRESENTATIVES   March 6, 2025   Mr. Joyce of Pennsylvania  (for himself and  Mrs. Trahan ) introduced the following bill; which was referred to the  Committee on Energy and Commerce , and in addition to the Committee on  Ways and Means , for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned   A BILL
To amend title XVIII of the Social Security Act to facilitate patient access to certain pediatric technologies.
1.
Short title
This Act may be cited as the   Access to Pediatric Technologies Act of 2025  .
2.
Facilitating access to pediatric technologies
(a)
In general
Section 1848 of the Social Security Act ( 42 U.S.C. 1395w–4 ) is amended by adding at the end the following new subsection:
(u)
Facilitating access to pediatric technologies
(1)
In general
For each qualifying pediatric technology (as defined in paragraph (4)) furnished on or after January 1, 2026, the Secretary shall, upon receipt of a manufacturer request under paragraph (3), establish national relative value units under the physician fee schedule established under this section, to the extent no such national relative value units have been established for such qualifying pediatric technology under such fee schedule.
(2)
Payment methodology
The Secretary shall establish national relative value units for a qualifying pediatric technology under this subsection—
(A)
in accordance with the payment methodology established under this section and applicable regulations; and
(B)
using available data related to the qualifying pediatric technology, which may include applicable contractor pricing information, claims data, time and motion studies, invoice information, or other information used by the Secretary in establishing payment rates.
(3)
Implementation
(A)
In general
Upon written request to the Secretary from the manufacturer of a qualifying pediatric technology, the Secretary shall establish national relative value units under paragraph (1) through the annual rulemaking process for the physician fee schedule established under this section, in accordance with the timeline described in subparagraph (B).
(B)
Timeline
(i)
In the case where the Secretary receives a request under this paragraph on or before May 1 of a given year from a manufacturer with respect to a qualifying pediatric technology of the manufacturer, the Secretary shall establish national relative value units for the qualifying pediatric technology in the rulemaking process during that year for the physician fee schedule established under this section.
(ii)
In the case where the Secretary receives a request under this paragraph after May 1 of a given year from a manufacturer with respect to a qualifying pediatric technology of the manufacturer, the Secretary shall establish national relative value units for the qualifying pediatric technology in the rulemaking process during the following year for the physician fee schedule established under this section.
(C)
Content of manufacturer requests
A manufacturer submitting a request under paragraph with respect to a qualifying pediatric technology of the manufacturer shall include in such request information to verify that the technology is a qualifying pediatric technology and to allow the Secretary to establish national relative value units for such technology, including (to the extent available) contractor pricing information, claims data, time and motion studies, invoice information, or other relevant information.
(4)
Qualifying pediatric technology defined
In this subsection, the term  qualifying pediatric technology  means a medical device that is—
(A)
covered under this title;
(B)
approved, cleared, or authorized under section 510(k), 513(f)(2), or 515 of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 360(k) , 360c(f)(2), 360e);
(C)
described by a temporary Level I HCPCS Code intended for emerging technologies, services, or procedures; and
(D)
(i)
used as part of a procedure predominantly performed on pediatric patients; or
(ii)
has otherwise been specifically designed for safe and effective use in pediatric populations.
(5)
Rule of construction
Nothing in this subsection shall be construed to require coverage of a qualifying pediatric technology under this title or alter the requirements of section 1862(a)(1)(A).
 .