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In the law of the United States, the Code of Federal Regulations (CFR) is the codification of the general and permanent regulations promulgated by the executive departments and agencies of the federal government of the United States. The CFR is divided into 50 titles that represent broad areas subject to federal regulation.
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Chapter 2 (1 CFR 51) concerns the incorporation by reference of outside documents into the Federal Register, thereby making them a part of the Federal Register. Regulations include the circumstances under which the Director of the Federal Register will approve incorporation, how to request approval, which publications are eligible, the proper language for citing incorporated publications, and ...
Fannie Mae, or the Federal National Mortgage Association (FNMA) Freddie Mac, or the Federal Home Loan Mortgage Corporation (FHLMC) The National Gallery of Art; The Smithsonian Institution (SI) is an independent establishment of the United States created by an act of Congress on August 10, 1846. The SI conducts scientific and scholarly research ...
Title 50 of the Code of Federal Regulations This page was last edited on 28 December 2022, at 18:39 (UTC). Text ...
The Federal Register system of publication was created on July 26, 1935, under the Federal Register Act. [4] [14] The first issue of the Federal Register was published on March 16, 1936. [15] In 1946 the Administrative Procedure Act required agencies to publish more information related to their rulemaking documents in the Federal Register. [16]
Federal Retirement Thrift Investment Board: VIII: 1800–1899: Office of Special Counsel: IX: 1900–1999: Appalachian Regional Commission: XI: 2100–2199: Armed Forces Retirement Home: XIV: 2400–2499: Federal Labor Relations Authority, General Counsel of the Federal Labor Relations Authority and Federal Service Impasses Panel: XV: 2500–2599
Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP). [1] It is divided into three chapters: Chapter I — Food and Drug Administration