Title 42The Public Health and WelfareRelease 119-73

§16041 Nuclear facility and materials security

Title 42 › Chapter CHAPTER 149— - NATIONAL ENERGY POLICY AND PROGRAMS › Subchapter SUBCHAPTER VI— - NUCLEAR MATTERS › Part Part C— - Nuclear Security › § 16041

Last updated Apr 6, 2026|Official source

Summary

The Nuclear Regulatory Commission must assign a Federal security coordinator to each of its regions within 18 months after August 8, 2005. Each coordinator must talk with the Commission and Federal, State, and local officials about threats, watch certain kinds of facilities to make sure their security matches the current threat level and security plans, and help match up private security forces with government authorities when needed. For any licensed nuclear power plant that has more than 15,000,000 people living within 50 miles (by the 2000 census), the Commission must require backup power for the plant’s emergency notification system, including sirens, if the alternating current supply inside the 10-mile emergency planning zone is lost, and this requirement must be in place within 18 months after August 8, 2005. Within 18 months after August 8, 2005, the Commission must issue final rules to carry out these duties and the changes made by this law. The rules must define the term “discrete source,” work with States as much as possible, and use model State standards that existed on August 8, 2005. The rules must include a transition plan for how regulatory authority over byproduct material will move between the Commission and States, and they must say when a State can have that authority. A State agreement already in place will count for newer definitions of byproduct material if the Governor certifies on the plan’s publication date that the State’s licensing program is adequate and that the State will keep enforcing it. The Commission must consider how rules affect the supply of radiopharmaceuticals to doctors and patients. The Commission may grant waivers for requirements about byproduct material if the waiver still protects public health, safety, and security, but it cannot waive certain amendments and some waivers end after 1 year or 4 years as specified. Any waiver must be published in the Federal Register. Definitions: - discrete source — a specific kind of radioactive source the Commission will define for the rules. - byproduct material — the materials described in paragraphs (3) and (4) of section 2014(e) of this title.

Full Legal Text

Title 42, §16041

The Public Health and Welfare — Source: USLM XML via OLRC

(a)(1)
(3)(A)Not later than 18 months after August 8, 2005, the Nuclear Regulatory Commission (referred to in this section as the “Commission”) shall assign a Federal security coordinator, under the employment of the Commission, to each region of the Commission.
(B)The Federal security coordinator shall be responsible for—
(i)communicating with the Commission and other Federal, State, and local authorities concerning threats, including threats against such classes of facilities as the Commission determines to be appropriate;
(ii)monitoring such classes of facilities as the Commission determines to be appropriate to ensure that they maintain security consistent with the security plan in accordance with the appropriate threat level; and
(iii)assisting in the coordination of security measures among the private security forces at such classes of facilities as the Commission determines to be appropriate and Federal, State, and local authorities, as appropriate.
(b)For any licensed nuclear power plants located where there is a permanent population, as determined by the 2000 decennial census, in excess of 15,000,000 within a 50-mile radius of the power plant, not later than 18 months after August 8, 2005, the Commission shall require that backup power to be available for the emergency notification system of the power plant, including the emergency siren warning system, if the alternating current supply within the 10-mile emergency planning zone of the power plant is lost.
(c)
(e)(1)
(4)(A)(i)Not later than 18 months after August 8, 2005, the Commission, after consultation with States and other stakeholders, shall issue final regulations establishing such requirements as the Commission determines to be necessary to carry out this section and the amendments made by this section.
(ii)The regulations shall include a definition of the term “discrete source” for purposes of paragraphs (3) and (4) of section 2014(e) of this title.
(B)In promulgating regulations under paragraph (1),11 So in original. Probably should be “subparagraph (A),”. the Commission shall, to the maximum extent practicable—
(i)cooperate with States; and
(ii)use model State standards in existence on August 8, 2005.
(C)(i)In this paragraph, the term “byproduct material” has the meaning given the term in paragraphs (3) and (4) of section 2014(e) of this title.
(ii)To facilitate an orderly transition of regulatory authority with respect to byproduct material, the Commission, in issuing regulations under subparagraph (A), shall prepare and publish a transition plan for—
(I)States that have not, before the date on which the plan is published, entered into an agreement with the Commission under section 2021(b) of this title; and
(II)States that have entered into an agreement with the Commission under that section before the date on which the plan is published.
(iii)The transition plan under clause (ii) shall include—
(I)a description of the conditions under which a State may exercise authority over byproduct material; and
(II)a statement of the Commission that any agreement covering byproduct material, as defined in paragraph (1) or (2) of section 2014(e) of this title, entered into between the Commission and a State under section 2021(b) of this title before the date of publication of the transition plan shall be considered to include byproduct material, as defined in paragraph (3) or (4) of section 2014(e) of this title, if the Governor of the State certifies to the Commission on the date of publication of the transition plan that—
(aa)the State has a program for licensing byproduct material, as defined in paragraph (3) or (4) of section 2014(e) of this title, that is adequate to protect the public health and safety, as determined by the Commission; and
(bb)the State intends to continue to implement the regulatory responsibility of the State with respect to the byproduct material.
(D)In promulgating regulations under subparagraph (A), the Commission shall consider the impact on the availability of radiopharmaceuticals to—
(i)physicians; and
(ii)patients the medical treatment of which relies on radiopharmaceuticals.
(5)(A)Except as provided in subparagraph (B), the Commission may grant a waiver to any entity of any requirement under this section or an amendment made by this section with respect to a matter relating to byproduct material (as defined in paragraphs (3) and (4) of section 2014(e) of this title) if the Commission determines that the waiver is in accordance with the protection of the public health and safety and the promotion of the common defense and security.
(B)(i)The Commission may not grant a waiver under subparagraph (A) with respect to—
(I)any requirement under the amendments made by subsection (c)(1);
(II)a matter relating to an importation into, or exportation from, the United States for a period ending after the date that is 1 year after August 8, 2005; or
(III)any other matter for a period ending after the date that is 4 years after August 8, 2005.
(ii)The Commission shall terminate any waiver granted to a State under subparagraph (A) if the Commission determines that—
(I)the State has entered into an agreement with the Commission under section 2021(b) of this title;
(II)the agreement described in subclause (I) covers byproduct material (as described in paragraph (3) or (4) of section 2014(e) of this title); and
(III)the program of the State for licensing such byproduct material is adequate to protect the public health and safety.
(C)The Commission shall publish in the Federal Register a notice of any waiver granted under this subsection.

Legislative History

Notes & Related Subsidiaries

Editorial Notes

References in Text

For references to “the

Amendments

made by this section”, “an amendment made by this section”, and “the

Amendments

made by subsection (c)(1)”, appearing in subsecs. (e)(4)(A)(i), (e)(5)(A), and (e)(5)(B)(i)(I), respectively, see Codification note below. Codification Section is comprised of section 651 of Pub. L. 109–58. Subsec. (a)(1), (2) of section 651 of Pub. L. 109–58 enacted section 2210d and 2210e of this title, subsec. (c)(1) of section 651 of Pub. L. 109–58 amended section 2051 of this title, subsecs. (c)(2) to (5) and (d) of section 651 of Pub. L. 109–58 enacted sections 2210f to 2210h and 2015c of this title, and subsec. (e)(1) to (3) of section 651 of Pub. L. 109–58 amended section 2014, 2021, 2021b, and 2111 of this title.

Reference

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Citation

42 U.S.C. § 16041

Title 42The Public Health and Welfare

Last Updated

Apr 6, 2026

Release point: 119-73