Federal
Newborn Screening Saves Lives Reauthorization Act of 2021
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II
117TH CONGRESS
1ST SESSION
S. 350
To amend the Public Health Service Act to reauthorize certain programs
under part A of title XI of such Act relating to genetic diseases, and
for other purposes.
IN THE SENATE OF THE UNITED STATES
FEBRUARY 22, 2021
Ms. HASSAN (for herself and Mr. WICKER) introduced the following bill; which
was read twice and referred to the Committee on Health, Education,
Labor, and Pensions
A BILL
To amend the Public Health Service Act to reauthorize cer-
tain programs under part A of title XI of such Act
relating to genetic diseases, and for other purposes.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
3
This Act may be cited as the ‘‘Newborn Screening
4
Saves Lives Reauthorization Act of 2021’’.
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SEC. 2. IMPROVED NEWBORN AND CHILD SCREENING AND
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FOLLOW-UP FOR HERITABLE DISORDERS.
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(a) PURPOSES.—Section 1109(a) of the Public
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Health Service Act (42 U.S.C. 300b–8(a)) is amended—
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(1) in paragraph (1), by striking ‘‘enhance, im-
1
prove or’’ and inserting ‘‘facilitate, enhance, im-
2
prove, or’’;
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(2) by amending paragraph (3) to read as fol-
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lows:
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‘‘(3) to develop, and deliver to parents, families,
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and patient advocacy and support groups, edu-
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cational programs that—
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‘‘(A) address newborn screening coun-
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seling, testing (including newborn screening
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pilot studies), follow-up, treatment, specialty
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services, and long-term care;
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‘‘(B) assess the target audience’s current
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knowledge, incorporate health communications
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strategies, and measure impact; and
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‘‘(C) are at appropriate literacy levels;’’;
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and
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(3) in paragraph (4)—
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(A) by striking ‘‘followup’’ and inserting
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‘‘follow-up’’; and
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(B) by inserting before the semicolon at
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the end the following: ‘‘, including re-engaging
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patients who have not received recommended
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follow-up services and supports’’.
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(b) APPROVAL FACTORS.—Section 1109(c) of the
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Public Health Service Act (42 U.S.C. 300b–8(c)) is
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amended—
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(1) by striking ‘‘or will use’’ and inserting ‘‘will
4
use’’; and
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(2) by inserting ‘‘, or will use amounts received
6
under such grant to enhance capacity and infra-
7
structure to facilitate the adoption of,’’ before ‘‘the
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guidelines and recommendations’’.
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SEC. 3. ADVISORY COMMITTEE ON HERITABLE DISORDERS
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IN NEWBORNS AND CHILDREN.
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Section 1111 of the Public Health Service Act (42
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U.S.C. 300b–10) is amended—
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(1) in subsection (b)—
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(A) in paragraph (5), by inserting ‘‘and
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adopt process improvements’’ after ‘‘take ap-
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propriate steps’’;
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(B) in paragraph (7) by striking ‘‘and’’ at
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the end;
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(C) by redesignating paragraph (8) as
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paragraph (9);
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(D) by inserting after paragraph (7) the
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following:
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‘‘(8) develop, maintain, and publish on a pub-
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licly accessible website consumer-friendly materials
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detailing—
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‘‘(A) the uniform screening panel nomina-
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tion process, including data requirements,
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standards, and the use of international data in
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nomination submissions; and
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‘‘(B) the process for obtaining technical as-
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sistance for submitting nominations to the uni-
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form screening panel and detailing the in-
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stances in which the provision of technical as-
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sistance would introduce a conflict of interest
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for members of the Advisory Committee; and’’;
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and
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(E) in paragraph (9), as redesignated—
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(i) by redesignating subparagraphs
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(K) and (L) as subparagraphs (L) and
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(M), respectively; and
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(ii) by inserting after subparagraph
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(J) the following:
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‘‘(K) the appropriate and recommended
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use of safe and effective genetic testing by
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health care professionals in newborns and chil-
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dren with an initial diagnosis of a disease or
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condition characterized by a variety of genetic
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causes and manifestations;’’; and
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(2) in subsection (g)—
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(A) in paragraph (1) by striking ‘‘2019’’
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and inserting ‘‘2026’’; and
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(B) in paragraph (2) by striking ‘‘2019’’
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and inserting ‘‘2026’’.
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SEC. 4. CLEARINGHOUSE OF NEWBORN SCREENING INFOR-
8
MATION.
9
Section 1112(c) of the Public Health Service Act (42
10
U.S.C. 300b–11(c)) is amended by striking ‘‘and supple-
11
ment, not supplant, existing information sharing efforts’’
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and inserting ‘‘and complement other Federal newborn
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screening information sharing activities’’.
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SEC. 5. LABORATORY QUALITY AND SURVEILLANCE.
15
Section 1113 of the Public Health Service Act (42
16
U.S.C. 300b–12) is amended—
17
(1) in subsection (a)—
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(A) in paragraph (1)—
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(i) by striking ‘‘performance evalua-
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tion services,’’ and inserting ‘‘development
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of new screening tests,’’; and
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(ii) by striking ‘‘and’’ at the end;
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(B) in paragraph (2)—
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(i) by striking ‘‘performance test ma-
1
terials’’ and inserting ‘‘test performance
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materials’’; and
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(ii) by striking the period at the end
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and inserting ‘‘; and’’; and
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(C) by adding at the end the following:
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‘‘(3) performance evaluation services to enhance
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disease detection, including the development of tools,
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resources, and infrastructure to improve data anal-
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ysis, test result interpretation, data harmonization,
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and dissemination of laboratory best practices.’’; and
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(2) by amending subsection (b) to read as fol-
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lows:
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‘‘(b) SURVEILLANCE ACTIVITIES.—The Secretary,
14
acting through the Director of the Centers for Disease
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Control and Prevention, and taking into consideration the
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expertise of the Advisory Committee on Heritable Dis-
17
orders in Newborns and Children established under sec-
18
tion 1111, shall provide for the coordination of national
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surveillance activities, including—
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‘‘(1) standardizing data collection and reporting
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through the use of electronic and other forms of
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health records to achieve real-time data for tracking
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and monitoring the newborn screening system, from
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the initial positive screen through diagnosis and
1
long-term care management; and
2
‘‘(2) by promoting data sharing linkages be-
3
tween State newborn screening programs and State-
4
based birth defects and developmental disabilities
5
surveillance programs to help families connect with
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services to assist in evaluating long-term outcomes.’’.
7
SEC. 6. HUNTER KELLY RESEARCH PROGRAM.
8
Section 1116 of the Public Health Service Act (42
9
U.S.C. 300b–15) is amended—
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(1) in subsection (a)(1)—
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(A) in the matter preceding subparagraph
12
(A), by striking ‘‘may’’ and inserting ‘‘shall’’;
13
and
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(B) in subparagraph (D)—
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(i) by inserting ‘‘, or with a high prob-
16
ability of being recommended by,’’ after
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‘‘recommended by’’; and
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(ii) by striking ‘‘that screenings are
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ready for nationwide implementation’’ and
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inserting ‘‘that reliable newborn screening
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technologies are piloted and ready for
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use’’; and
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(2) by amending subsection (b) to read as fol-
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lows:
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‘‘(b) FUNDING.—In carrying out the research pro-
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gram under this section, the Secretary and the Director
2
shall ensure that entities receiving funding through the
3
program will provide assurances, as practicable, that such
4
entities will work in consultation with State departments
5
of health, as appropriate.’’.
6
SEC. 7. AUTHORIZATION OF APPROPRIATIONS FOR NEW-
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BORN SCREENING PROGRAMS AND ACTIVI-
8
TIES.
9
Section 1117 of the Public Health Service Act (42
10
U.S.C. 300b–16) is amended—
11
(1) in paragraph (1)—
12
(A) by striking ‘‘$11,900,000’’ and insert-
13
ing ‘‘$31,000,000’’;
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(B) by striking ‘‘2015’’ and inserting
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‘‘2022’’; and
16
(C) by striking ‘‘2019’’ and inserting
17
‘‘2026’’; and
18
(2) in paragraph (2)—
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(A) by striking ‘‘$8,000,000’’ and inserting
20
‘‘$29,650,000’’;
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(B) by striking ‘‘2015’’ and inserting
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‘‘2022’’; and
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(C) by striking ‘‘2019’’ and inserting
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‘‘2026’’.
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SEC. 8. INSTITUTIONAL REVIEW BOARDS; ETHICS GUID-
1
ANCE PROGRAM.
2
Section 12 of the Newborn Screening Saves Lives Re-
3
authorization Act of 2014 (42 U.S.C. 289 note) is amend-
4
ed to read as follows:
5
‘‘SEC. 12. INSTITUTIONAL REVIEW BOARDS; ETHICS GUID-
6
ANCE PROGRAM.
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‘‘Research on nonidentified newborn dried blood spots
8
shall be considered secondary research (within the mean-
9
ing of section 46.104(d)(4) of title 45, Code of Federal
10
Regulations (or successor regulations)) with nonidentified
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biospecimens for purposes of federally funded research
12
conducted pursuant to the Public Health Service Act (42
13
U.S.C. 201 et seq.).’’.
14
SEC. 9. NAM REPORT ON THE MODERNIZATION OF NEW-
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BORN SCREENING.
16
(a) STUDY.—Not later than 60 days after the date
17
of the enactment of this Act, the Secretary of Health and
18
Human Services shall seek to enter into an agreement
19
with the National Academy of Medicine (in this section
20
referred to as ‘‘NAM’’) (or if NAM declines to enter into
21
such an agreement, another appropriate entity) under
22
which NAM, or such other appropriate entity, agrees to
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conduct a study on the following:
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(1) The uniform screening panel review and
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recommendation processes to identify factors that
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impact decisions to add new conditions to the uni-
1
form screening panel, to describe challenges posed
2
by newly nominated conditions, including low-inci-
3
dence diseases, late onset variants, and new treat-
4
ments without long-term efficacy data.
5
(2) The barriers that preclude States from add-
6
ing new uniform screening panel conditions to their
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State screening panels with recommendations on re-
8
sources needed to help States implement uniform
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screening panel recommendations.
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(3) The current state of federally and privately
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funded newborn screening research with rec-
12
ommendations for optimizing the capacity of this re-
13
search, including piloting multiple prospective condi-
14
tions at once and addressing rare disease questions.
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(4) New and emerging technologies that would
16
permit screening for new categories of disorders, or
17
would make current screening more effective, more
18
efficient, or less expensive.
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(5) Technological and other infrastructure
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needs to improve timeliness of diagnosis and short-
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and long-term follow-up for infants identified
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through newborn screening and improve public
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health surveillance.
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(6) Current and future communication and edu-
1
cational needs for priority stakeholders and the pub-
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lic to promote understanding and knowledge of a
3
modernized newborn screening system with an em-
4
phasis on evolving communication channels and mes-
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saging.
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(7) The extent to which newborn screening
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yields better data on the disease prevalence for
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screened conditions and improves long-term out-
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comes for those identified through newborn screen-
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ing, including existing systems supporting such data
11
collection and recommendations for systems that
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would allow for improved data collection.
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(8) The impact on newborn morbidity and mor-
14
tality in States that adopt newborn screening tests
15
included on the uniform panel.
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(b) PUBLIC STAKEHOLDER MEETING.—In the course
17
of completing the study described in subsection (a), NAM
18
or such other appropriate entity shall hold not less than
19
one public meeting to obtain stakeholder input on the top-
20
ics of such study.
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(c) REPORT.—The agreement under subsection (a)
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shall require NAM, or such other appropriate entity, not
23
later than 18 months after the effective date of such
24
agreement, to submit to the Secretary of Health and
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Human Services and the appropriate committees of juris-
1
diction of Congress a report containing—
2
(1) the results of the study conducted under
3
subsection (a);
4
(2) recommendations to modernize the proc-
5
esses described in subsection (a)(1); and
6
(3) recommendations for such legislative and
7
administrative action as NAM, or such other appro-
8
priate entity, determines appropriate.
9
(d) AUTHORIZATION OF APPROPRIATIONS.—There is
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authorized to be appropriated $2,000,000 for the period
11
of fiscal years 2022 and 2023 to carry out this section.
12
Æ
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