A Conformity Assessment Body notified in accordance with this Regulation and other relevant Union harmonisation legislation.
Source: Article 3(22) of the EU AI Act
#EUAIActDefinitions
A Conformity Assessment Body notified in accordance with this Regulation and other relevant Union harmonisation legislation.
Source: Article 3(22) of the EU AI Act
#EUAIActDefinitions
A body that performs third-party Conformity Assessment activities, including testing, certification and inspection.
Source: Article 3(21) of the EU AI Act
#EUAIActDefinitions
The process of demonstrating whether the requirements set out in Chapter III, Section 2 relating to a High-Risk AI System have been fulfilled.
Source: Article 3(20) of the EU AI Act
#EUAIActDefinitions
The national authority responsible for setting up and carrying out the necessary procedures for the assessment, designation and notification of Conformity Assessment Bodies and for their monitoring.
Source: Article 3(19) of the EU AI Act
#EUAIActDefinitions
The ability of an AI System to achieve its Intended Purpose.
Source: Article 3(18) of the EU AI Act
#EUAIActDefinitions
Any measure aimed at preventing an AI System in the supply chain being made available on the market.
Source: Article 3(17) of the EU AI Act
#EUAIActDefinitions
Any measure aimed at achieving the return to the Provider or taking it out of service or disabling the use of an AI System made available to Deployers.
Source: Article 3(16) of the EU AI Act
#EUAIActDefinitions
The information provided by the Provider to inform the Deployer of, in particular, an AI System’s Intended Purpose and proper use.
Source: Article 3(15) of the EU AI Act
#EUAIActDefinitions
A component of a product or of an AI System which fulfils a safety function for that product or AI System, or the failure or malfunctioning of which endangers the health and safety of persons or property.
Source: Article 3(14) of the EU AI Act
#EUAIActDefinitions
The use for which an AI System is intended by the Provider, including the specific context and conditions of use, as specified in the information supplied by the Provider in the Instructions for Use, promotional or sales materials and statements, as well as in the technical documentation.
Source: Article 3(12) of the EU AI Act
#EUAIActDefinitions