21-U.S.C.-377

§377 – Revision of United States Pharmacopoeia; Development of Analysis and Mechanical and Physical Tests

Pathway

Title 21 > Chapter 9 > Subchapter VII > Part A > Section 377

Details

• Reference: Section 377
• Legend: §377 – Revision of United States Pharmacopoeia; Development of Analysis and Mechanical and Physical Tests
• USCode Year: 2013

Provision Content

The Secretary, in carrying into effect the provisions of this chapter, is authorized on and after July 12, 1943, to cooperate with associations and scientific societies in the revision of the United States Pharmacopoeia and in the development of methods of analysis and mechanical and physical tests necessary to carry out the work of the Food and Drug Administration.

(July 12, 1943, ch. 221, title II, 57 Stat. 500; 1953 Reorg. Plan No. 1, §5, eff. Apr. 11, 1953, 18 F.R. 2053, 67 Stat. 631.)

Codification

Section was enacted as part of the Labor-Federal Security Appropriation Act, 1944, and not as part of the Federal Food, Drug, and Cosmetic Act which comprises this chapter.

Transfer of Functions

For transfer of functions of Federal Security Administrator to Secretary of Health, Education, and Welfare [now Health and Human Services], and of Food and Drug Administration in the Department of Agriculture to Federal Security Agency, see notes set out under section 321 of this title.

U.S. Encyclopedia of Law Coverage

21-U.S.C.-371 in the Legal Encyclopedia: Drugs General Authority

In this entry about 21-U.S.C.-371, find legal reference material, bibliographies and premiere content related to drugs general authority in the American Encyclopedia of Law, presenting a comprehensive view of the United States drugs general authority-specific issues, written by authorities in the field.

Topic Map

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