§ 7331. Informed consent

205 words·~1 min read·/usc/title-38/section-7331

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The Secretary, upon the recommendation of the Under Secretary for Health and pursuant to the provisions of section 7334 of this title, shall prescribe regulations establishing procedures to ensure that all medical and prosthetic research carried out and, to the maximum extent practicable, all patient care furnished under this title shall be carried out only with the full and informed consent of the patient or subject or, in appropriate cases, a representative thereof.

(Added Pub. L. 94–581, title I, § 111(a)(1), Oct. 21, 1976, 90 Stat. 2849, § 4131; renumbered § 7331 and amended Pub. L. 102–40, title IV, §§ 401(a)(4)(A), 402(d)(1), 403(a)(1), May 7, 1991, 105 Stat. 221, 239; Pub. L. 102–405, title III, § 302(c)(1), Oct. 9, 1992, 106 Stat. 1984.)

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Pub. L. 94–581, title I, § 111(a)(1)
90 Stat. 2849
Pub. L. 102–40, title IV
105 Stat. 221
Pub. L. 102–405, title III, § 302(c)(1)
106 Stat. 1984
Pub. L. 102–405
Pub. L. 102–40, § 401(a)(4)(A)
section 4131 of this title
Pub. L. 102–40, § 403(a)(1)
Pub. L. 102–40, § 402(d)(1)
section 211 of Pub. L. 94–581

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§ 7331

Informed consent

Fed. Reg.×16

U.S.C.×2

U.S.C.§ 7334

U.S.C.§ 111

Pub. L.Pub. L. 94–581, title I, § 111(a)(1)

Stat.90 Stat. 2849

Pub. L.Pub. L. 102–40, title IV

Stat.105 Stat. 221

Pub. L.Pub. L. 102–405, title III, § 302(c)(1)

Cites 14 · showing 7Cited by 18 across 2 sources