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42 U.S.C. § 2142 — Domestic medical isotope production

submitted 80 years ago by Pub. L. 112-239 to r/title-42-THE-PUBLIC-HEALTH-AND-WELFARE · 291 words · no verdicts yet

in plain englishAI-generated · not legal advice

The Commission may authorize highly enriched uranium as a medical-isotope production target only when no usable alternative exists, the recipient promises to switch when one becomes usable, and the Secretary of Energy certifies that the United States is supporting an alternative. The section defines the relevant targets, uranium, and medical isotopes.

(a) The Commission may issue a license or amend an existing license to allow highly enriched uranium to be used as a target for producing medical isotopes in a nuclear reactor in the United States only if all of these additional conditions are met:

(1) The Commission determines that—

(A) the reactor has no alternative medical-isotope production target that can be used in it; and

(B) the proposed recipient promises that, whenever such an alternative can be used in the reactor, it will use the alternative instead of highly enriched uranium; and

(2) the Secretary of Energy certifies that the United States Government is actively supporting development of an alternative target that can be used in that reactor.

(b) In this section—

(1) “Alternative medical isotope production target” means a nuclear-reactor target enriched to less than 20 percent U–235.

(2) A target “can be used” in a nuclear research or test reactor if—

(A) the Department of Energy’s Reduced Enrichment Research and Test Reactor Program has qualified the target; and

(B) using it would allow the large majority of ongoing and planned experiments and medical-isotope production to take place in the reactor without a large percentage increase in the reactor’s total operating cost.

(3) “Highly enriched uranium” means uranium enriched to 20 percent or more U–235.

(4) “Medical isotope” includes molybdenum-99, iodine-131, xenon-133, and other radioactive materials used to produce a radiopharmaceutical for diagnostic or therapeutic procedures or for research and development. This section does not otherwise define “radiopharmaceutical,” “diagnostic,” “therapeutic,” “research,” or “development.”

the actual law source: uscode.house.gov ↗public domain
(a)

The Commission may issue a license, or grant an amendment to an existing license, for the use in the United States of highly enriched uranium as a target for medical isotope production in a nuclear reactor, only if, in addition to any other requirement of this chapter—

(1)

the Commission determines that—

(A)

there is no alternative medical isotope production target that can be used in that reactor; and

(B)

the proposed recipient of the medical isotope production target has provided assurances that, whenever an alternative medical isotope production target can be used in that reactor, it will use that alternative in lieu of highly enriched uranium; and

(2)

the Secretary of Energy has certified that the United States Government is actively supporting the development of an alternative medical isotope production target that can be used in that reactor.

(b)

As used in this section—

(1)

the term “alternative medical isotope production target” means a nuclear reactor target which is enriched to less than 20 percent of the isotope U–235;

(2)

a target “can be used” in a nuclear research or test reactor if—

(A)

the target has been qualified by the Reduced Enrichment Research and Test Reactor Program of the Department of Energy; and

(B)

use of the target will permit the large majority of ongoing and planned experiments and medical isotope production to be conducted in the reactor without a large percentage increase in the total cost of operating the reactor;

(3)

the term “highly enriched uranium” means uranium enriched to 20 percent or more in the isotope U–235; and

(4)

the term “medical isotope” includes molybdenum-99, iodine-131, xenon-133, and other radioactive materials used to produce a radiopharmaceutical for diagnostic or therapeutic procedures or for research and development.

Source credit: (Aug. 1, 1946, ch. 724, title I, § 112, as added Pub. L. 112–239, div. C, title XXXI, § 3176(a), Jan. 2, 2013, 126 Stat. 2215; Pub. L. 113–66, div. C, title XXXI, § 3144, Dec. 26, 2013, 127 Stat. 1071.)

history & why it existsrecord from the source credit
  • 1946Enacted · Pub. L. 112-239 · 126 Stat. 2215
  • 2013Amended · Pub. L. 113-66 · 127 Stat. 1071

A history note hasn’t been published yet. The record shows enactment by Pub. L. 112-239 on 1946-08-01.

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