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IEC SRD 63234-1:2020 provides a descriptive framework and template for the economic evaluation of the implementation of technology-supported home healthcare or wellness services, or AAL services that support communications, transportation, etc. as defined in a series of AAL use cases. The financial analysis is completed from the point of view of the healthcare services funder, aged care services…

This document describes requirements for collections of metadata about data elements and their containing models and datasets in a healthcare environment. The collection can serve as a repository or as dictionary describing a set of items in use in a particular domain, organisation or product for reference, or it can additionally serve as a registry, supporting the development and communication…

This Standard specifies minimum requirements in protecting human values and incorporating ethics in the design and use of automated decision systems. This Standard is limited to artificial intelligence (AI) using machine learning for automated decisions. This Standard applies to all organizations, including public and private companies, government entities, and not-for-profit organizations. It…

This document specifies the tasks, roles, and key skills, requirements and competencies for personnel involved in terminology services in healthcare organizations. This document specifies — terminology services in healthcare organizations including the selection, authoring, and deployment and use of terminology subsets and maps; developing and managing terminology management processes…

Artificial intelligence (AI) is continuously making inroads into domains previously reserved to humans. Robots support workers in the manufacturing sector; digital assistants automate office tasks; intelligent appliances order food based on owners’ preferences or control lighting and temperature in the home in preparation of their arrival. Increasingly sophisticated algorithms have the potential…

This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the nature and duration of their contact with the body; — the evaluation of existing relevant data from all sources; — the identification of gaps in the available data…

IEC TS 62361-102:2018(E) outlines a technical approach for achieving effective information exchange between power system installations governed by IEC 61850 and business systems integrated with IEC CIM standard data exchanges, based on a selected specific set of use cases, but also with the goal of creating a framework that will extend successfully to other use cases in the future. This document…

1.1 Facilities 1.1.1 Types of facilities 1.1.1.1 This Standard addresses the establishment and implementation of ALs for Class I nuclear facilities and uranium mines and mills. Notes: 1) In this Standard, any type of Class I nuclear facility or uranium mine and mill is included in the term “nuclear facilities”. 2) Conventional waste management facilities (e.g., landfills, incinerators,…

1.1 Scope of MLR multipart standard The primary purpose of this International Standard is to specify metadata elements and their attributes for the description of learning resources. This includes the rules governing the identification of data elements and the specification of their attributes. This International Standard provides data elements for the description of learning resources and…

1.1 Scope of MLR International Standard The primary purpose of this International Standard is to specify metadata elements and their attributes for the description of learning resources. This includes the rules governing the identification of data elements and the specification of their attributes. This International Standard provides data elements for the description of learning resources and…