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42 U.S.C. § 283ePlan for use of animals in research

submitted 82 years ago by Pub. L. 103-43 to r/title-42-THE-PUBLIC-HEALTH-AND-WELFARE · 451 words · no verdicts yet

in plain englishAI-generated · not legal advice

NIH must create a plan to reduce animal use in research, find alternatives, and cut animal pain. The Director must send this plan to Congress, keep updating it, and share proven alternative methods with scientists. A special committee of agency representatives advises on the plan.

(a) Preparation: After consulting with the committee set up under subsection (e), the Director of NIH must prepare a plan. The plan covers NIH conducting or supporting research into (A) ways to do biomedical research and experiments without using animals; (B) ways to reduce the number of animals used; (C) ways to cause animals less pain and distress; and (D) ways that use marine life other than marine mammals. The plan must also cover (2) establishing whether these methods are valid and reliable, (3) encouraging scientists to accept methods proven valid and reliable, and (4) training scientists to use those proven methods. (b) Submission to Congressional committees: By October 1, 1993, the Director had to submit this plan to the House Committee on Energy and Commerce and the Senate Committee on Labor and Human Resources, and start putting the plan into action. (c) Periodic review and revision: The Director must periodically review the plan and revise it as needed. Any revision must be described in the next biennial report under section 283 of this title that comes out after the revision is made. (d) Dissemination of information: The Director must take appropriate steps to tell scientists and others who use animals in biomedical or behavioral research about which methods have been found valid and reliable under subsection (a)(2). (e) Interagency Coordinating Committee on the Use of Animals in Research: The Director must set up a committee within NIH called the Interagency Coordinating Committee on the Use of Animals in Research. This Committee advises the Director on preparing the plan required by subsection (a). It is made up of the directors of each national research institute (or their designees), plus representatives from the Environmental Protection Agency, the Food and Drug Administration, the Consumer Product Safety Commission, the National Science Foundation, and any other agencies the Director thinks are appropriate. Among those representatives, at least one must be a veterinarian with expertise in laboratory-animal medicine.
the actual law source: uscode.house.gov ↗public domain
(a) Preparation

The Director of NIH, after consultation with the committee established under subsection (e), shall prepare a plan—

(1)

for the National Institutes of Health to conduct or support research into—

(A)

methods of biomedical research and experimentation that do not require the use of animals;

(B)

methods of such research and experimentation that reduce the number of animals used in such research;

(C)

methods of such research and experimentation that produce less pain and distress in such animals; and

(D)

methods of such research and experimentation that involve the use of marine life (other than marine mammals);

(2)

for establishing the validity and reliability of the methods described in paragraph (1);

(3)

for encouraging the acceptance by the scientific community of such methods that have been found to be valid and reliable; and

(4)

for training scientists in the use of such methods that have been found to be valid and reliable.

(b) Submission to Congressional committees

Not later than October 1, 1993, the Director of NIH shall submit to the Committee on Energy and Commerce of the House of Representatives, and to the Committee on Labor and Human Resources of the Senate, the plan required in subsection (a) and shall begin implementation of the plan.

(c) Periodic review and revision

The Director of NIH shall periodically review, and as appropriate, make revisions in the plan required under subsection (a). A description of any revision made in the plan shall be included in the first biennial report under section 283 of this title that is submitted after the revision is made.

(d) Dissemination of information

The Director of NIH shall take such actions as may be appropriate to convey to scientists and others who use animals in biomedical or behavioral research or experimentation information respecting the methods found to be valid and reliable under subsection (a)(2).

(e) Interagency Coordinating Committee on the Use of Animals in Research
(1)

The Director of NIH shall establish within the National Institutes of Health a committee to be known as the Interagency Coordinating Committee on the Use of Animals in Research (in this subsection referred to as the “Committee”).

(2)

The Committee shall provide advice to the Director of NIH on the preparation of the plan required in subsection (a).

(3)

The Committee shall be composed of—

(A)

the Directors of each of the national research institutes (or the designees of such Directors); and

(B)

representatives of the Environmental Protection Agency, the Food and Drug Administration, the Consumer Product Safety Commission, the National Science Foundation, and such additional agencies as the Director of NIH determines to be appropriate, which representatives shall include not less than one veterinarian with expertise in laboratory-animal medicine.

Source credit: (July 1, 1944, ch. 373, title IV, § 404C, as added Pub. L. 103–43, title II, § 205(a), June 10, 1993, 107 Stat. 146; amended Pub. L. 112–74, div. F, title II, § 221(d)(2), Dec. 23, 2011, 125 Stat. 1090.)

history & why it existsrecord from the source credit
  • 1944Enacted · Pub. L. 103-43 · 107 Stat. 146
  • 2011Amended · Pub. L. 112-74 · 125 Stat. 1090

A history note hasn’t been published yet. The record shows enactment by Pub. L. 103-43 on 1944-07-01.

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