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v. t. e. Regulation of artificial intelligence is the development of public sector policies and laws for promoting and regulating artificial intelligence (AI). It is part of the broader regulation of algorithms. [1] [2] The regulatory and policy landscape for AI is an emerging issue in jurisdictions worldwide, including for international ...
The Federal Risk and Authorization Management Program ( FedRAMP) is a United States federal government -wide compliance program that provides a standardized approach to security assessment, authorization, and continuous monitoring for cloud products and services. [1]
Barr v. American Assn. of Political Consultants, Inc., No. 19-631, 591 U.S. ___ (2020) The Telephone Consumer Protection Act of 1991 ( TCPA) was passed by the United States Congress in 1991 and signed into law by President George H. W. Bush as Public Law 102-243. It amended the Communications Act of 1934. The TCPA is codified as 47 U.S.C. § 227.
Andrej Sokolow/dpa/AP. The Federal Trade Commission is investigating a recent Microsoft deal with artificial intelligence startup Inflection, according to a person familiar with the matter, as US ...
Know Your Customer (KYC) guidelines and regulations in financial services require professionals to verify the identity, suitability, and risks involved with maintaining a business relationship with a customer. The procedures fit within the broader scope of anti-money laundering (AML) and counter terrorism financing (CTF) regulations.
California lawmakers are considering legislation that would require artificial intelligence companies to test their systems and add safety measures so they can't be potentially manipulated to wipe ...
The report will explain the facts and reasons upon which the officer’s or employee’s belief rests and must be submitted to OPR. "Such reports are required by section 10.53(a) of the regulations governing practice, which are set out at 31 C.F.R. Part 10, and are published in pamphlet form as Treasury Department Circular No. 230."
Title 21 CFR Part 11 is the part of Title 21 of the Code of Federal Regulations that establishes the United States Food and Drug Administration (FDA) regulations on electronic records and electronic signatures (ERES). Part 11, as it is commonly called, defines the criteria under which electronic records and electronic signatures are considered ...