H.R. 3029House119th Congress (2025-2027)Passed House

To amend the Research and Development, Competition, and Innovation Act to support nucleic acid screening, and for other purposes.

Introduced April 28, 2025

AI-Generated Summary

Updated July 23, 2026 at 12:52 AM UTC

The Nucleic Acid Standards for Biosecurity Act amends the Research and Development, Competition, and Innovation Act to strengthen U.S. biosecurity by improving screening of synthetic nucleic acids. It directs the federal government to develop best‑practice guidelines, technical standards, and measurement research for nucleic‑acid‑synthesis screening, and to bring together stakeholders to create consensus roadmaps. The law also provides funding for the National Institute of Standards and Technology to carry out this work.

Key Provisions

  • Adds a new subparagraph requiring the development of best practices, guidelines, and technical standards for managing risks in engineering biology and biomanufacturing, including AI‑related risks.
  • Creates a new subsection that tasks the Director (with input from other federal agencies) to conduct research and develop standards for nucleic‑acid‑synthesis screening, covering testing accuracy, security controls, implementation guidance, conformity‑assessment practices, and methods to evaluate effectiveness.
  • Requires the Director to convene a consortium of industry, academia, nonprofits, and customers to set consensus priorities, develop best‑practice roadmaps, and periodically update them.
  • Mandates a report to the Senate Commerce, Science, and Transportation Committee and the House Science, Space, and Technology Committee within 18 months of the consortium’s first meeting.
  • Authorizes $5 million per fiscal year from 2027 through 2031 for the National Institute of Standards and Technology to fund these activities.

Legislative Activity

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12 earlier actions
SenateIntro Referral Latest Action

Received in the Senate and Read twice and referred to the Committee on Commerce, Science, and Transportation.

July 21, 2026

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HouseIntro Referral

Introduced in House

April 28, 2025

HouseIntro Referral

Referred to the House Committee on Science, Space, and Technology.

April 28, 2025

HouseCommittee

Committee Consideration and Mark-up Session Held

April 29, 2025

HouseCommittee

Ordered to be Reported by Voice Vote.

April 29, 2025

HouseCommittee

Reported by the Committee on Science, Space, and Technology. H. Rept. 119-751.

July 16, 2026

HouseCalendars

Placed on the Union Calendar, Calendar No. 654.

July 16, 2026

HouseFloor

Mr. Babin moved to suspend the rules and pass the bill, as amended.

July 20, 2026 • 5:20 PM

HouseFloor

Considered under suspension of the rules. (consideration: CR H4666-4667)

July 20, 2026 • 5:20 PM

HouseFloor

DEBATE - The House proceeded with forty minutes of debate on H.R. 3029.

July 20, 2026 • 5:20 PM

HouseFloor

Passed/agreed to in House: On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote. (text: CR H4666)

July 20, 2026 • 5:27 PM

HouseFloor

On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote. (text: CR H4666)

July 20, 2026 • 5:27 PM

HouseFloor

Motion to reconsider laid on the table Agreed to without objection.

July 20, 2026 • 5:27 PM

SenateIntro Referral

Received in the Senate and Read twice and referred to the Committee on Commerce, Science, and Transportation.

July 21, 2026

Floor Debate

2 members

What members said about H.R. 3029 on the floor

1 Republican1 Democrat
Brian Babin
Rep. Brian BabinR-TX-36 · Jul 20, 2026

Madam Speaker, I move to suspend the rules and pass the bill (H.R. 3029) to amend the Research and Development, Competition, and Innovation Act to support nucleic acid screening, and for other…

Andrea Salinas
Rep. Andrea SalinasD-OR-6 · Jul 20, 2026

Madam Speaker, I yield myself the balance of my time. Madam Speaker, American biotech companies are leading a scientific revolution that is transforming our economy. In recent years, we have seen…

Bill Text

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Referred in SenateIssued July 21, 2026

IIB

119th CONGRESS

2d Session

H. R. 3029

IN THE SENATE OF THE UNITED STATES

July 21, 2026

Received; read twice and referred to the Committee on Commerce, Science, and Transportation

AN ACT

To amend the Research and Development, Competition, and Innovation Act to support nucleic acid screening, and for other purposes.

1.

Short title

This Act may be cited Nucleic Acid Standards for Biosecurity Act.

2.

Supporting nucleic acid screening

Section 10221 of the Research and Development, Competition, and Innovation Act (42 U.S.C. 18931; enacted as part of title II of division B of Public Law 117–167) is amended—

(1)

in subsection (a)(1)—

(A)

in subparagraph (C), by striking and after the semicolon;

(B)

by redesignating subparagraph (D) as subparagraph (E); and

(C)

by inserting after subparagraph (C) the following new subparagraph:

(D)

best practices, guidelines, and technical standards for risk management associated with engineering biology and biomanufacturing, including risks associated with the use of artificial intelligence; and

;

(2)

by redesignating subsections (b) and (c) as subsections (c) and (d), respectively; and

(3)

by inserting after subsection (a) the following new subsection:

(b)

Nucleic acid synthesis screening tools and standards

(1)

In general

The Director, in consultation with heads of Federal agencies the Director considers appropriate, shall carry out measurement research to support the development and improvement of best practices and technical standards for biosecurity measures related to nucleic acid synthesis, including the following:

(A)

Testing to improve the accuracy, efficacy, and reliability of screening for nucleic acid synthesis.

(B)

Best practices, including security and access controls, for operational security and managing sequence-of-concern databases to support such screening.

(C)

Technical implementation guidance to ensure such screening is effective and secure.

(D)

Conformity-assessment best practices and technical standards.

(E)

Methods to evaluate the impact and effectiveness of the implementation of subparagraphs (A) through (D).

(2)

Consortium

In carrying out this subsection, the Director shall convene a consortium of stakeholders, including industry, institutions of higher education, nonprofit organizations, and customers to carry out the following:

(A)

Develop and periodically update consensus priorities and best practices, as appropriate, for synthetic nucleic acid procurement screening mechanisms.

(B)

Develop roadmaps to inform the activities carried out under paragraph (1).

(3)

Report

Not later than 18 months after the first meeting of the consortium under paragraph (2), the Director shall submit to the Committee on Commerce, Science, and Transportation of the Senate and the Committee on Science, Space, and Technology of the House of Representatives a report summarizing the findings of the consortium.

(4)

Authorization of appropriations

Of the funds authorized to be appropriated for the National Institute of Standards and Technology pursuant to this section for scientific and technical research and services laboratory activities, there is authorized to be appropriated $5,000,000 for each of


fiscal years 2027 through 2031 to carry out this subsection.

.

Passed the House of Representatives July 20, 2026.

Kevin F. McCumber,

Clerk.