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The Federal Records Act was created following the recommendations of the Hoover Commission (1947-49). [1] It implemented one of the reforms proposed by Emmett Leahy in his October 1948 report on Records Management in the United States Government, with the goal of ensuring that all federal departments and agencies had a program for records management.
The Presidential and Federal Records Act Amendments of 2014 (Pub. L. 113–187 (text)) is a United States federal statute which amended the Presidential Records Act and Federal Records Act. Introduced as H.R. 1233 , it was signed into law by President Barack Obama on November 26, 2014.
Chapter 3 (1 CFR 300-399) addresses the Administrative Conference of the United States (ACUS), an independent agency established by the Administrative Conference Act. [17] The CFR states that the purposes of the ACUS are to facilitate cooperation between the federal government and the general public to ensure that regulations are most effective ...
The Federal Register Act originally provided for a complete compilation of all existing regulations promulgated prior to the first publication of the Federal Register, but was amended in 1937 to provide a codification of all regulations every five years. [7] The first edition of the CFR was published in 1938. [7]
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]
This is a chronological, but incomplete, list of United States federal legislation passed by the 57th through 106th United States Congresses, between 1901 and 2001. For the main article on this subject, see List of United States federal legislation.
The first volume of the CFR was published in 1939 with general applicability and legal effect in force June 1, 1938. [2] The Office of the Federal Register (OFR) began publishing yearly revisions for some titles in 1963 with legal effective dates of January 1 each year. By 1967 all 50 titles were updated annually and effective January 1.
Most of the Chapter I regulations are based on the Federal Food, Drug, and Cosmetic Act. Notable sections: 11 — electronic records and electronic signature related; 50 Protection of human subjects in clinical trials; 54 Financial disclosure by clinical investigators [2] 56 Institutional review boards that oversee clinical trials