IT in general

IEC 62325-451-10:2020 specifies a UML package for the Energy Consumption Data business process and its associated document contextual model, assembly model and XML schema for use within the European style electricity markets.

The relevant aggregate core components (ACCs) defined in IEC 62325-351 have been contextualised into aggregated business information entities (ABIEs) to satisfy the requirements of the European style market Energy Consumption Data business process.

The contextualised ABIEs have been assembled into the Energy Consumption Data document contextual model.

A related assembly model and an XML schema for the exchange of Energy Consumption information between market participants is automatically generated from the assembled document contextual model. The XML schema follows IEC Code Components management and copyright licensing.

ISO/TS 13972:2015:
(a) Describes requirements and recommended methods against which clinicians can gather, analyse and, specify the clinical context, content, and structure of Detailed Clinical Models.
(b) Defines Detailed Clinical Models (DCMs) in terms of an underlying logical model. They are logical models of clinical concepts and can be used to define and to structure clinical information.
(c) Describes requirements and principles for DCMs, meta-data, versioning, content and context specification, data element specification and data element relationships, and provide guidance and examples.
(d) Specifies DCM governance principles to ensure conceptual integrity of all DCM attributes and logical model accuracy.
(e) Describes DCM development and the methodology principles for use that will support the production of quality DCMs to minimize risk and ensure patient safety.

ISO/TR 19669:2017 specifies a use case development methodology, facilitated by a dynamic catalogue of re-usable components. Use cases are a basic tool in describing requirements for health and healthcare settings, service provision, information technology and software products. Use case development often follows a uniform template with components such as actors, roles, scenarios, event steps, actions, data objects/ elements and requirements statements. ISO/TR 19669:2017 includes a basic use case template and the methods of component identification, capture, cataloguing and re-use. This document also includes guidance for software designed to implement the methodology in the form of a use case authoring too.

ISO/TR 18307:2001, 3.51. Health informatics::Interoperability and compatibility in messaging and communication standards::Key characteristics

This Technical Report also considers the wider context of engagement of individuals in the management of their own health and healthcare, since this engagement is the primary driver for present-day growth of PHR systems and services internationally. This Technical Report includes: (a) a definition of a PHR; (b) a pragmatic multidimensional classification of PHRs; (c) an overview of the possible ways in which the inclusion and engagement of individuals in managing their health and healthcare impacts on the potential roles of the PHR, including scenarios for collaborative care between individuals and healthcare organizations.
The many kinds of end-user application that might be implemented and used to deliver PHR system functionality are outside the scope of this Technical Report.

ISO 18369-1:2017, 3.1.9.2.Ophthalmic optics::Contact lenses::Part 1: Vocabulary, classification system and recommendations for labelling specifications

This standard defines the common base requirements for Participants in a Service-Oriented Device Connectivity (SDC) System that comprises a network of point-of-care (PoC) medical devices and medical IT systems to improve effective, safe and secure contribution to a system function such as metric provisioning.

Within the context of the ISO/IEEE 11073(TM) family of standards for point-of-care medical device communication, a Participant Model derived from the ISO/IEEE11073-10201 Domain Information Model is provided in this standard. The Participant Model specifies the structure of medical information objects. This standard also defines an abstract Communication Model to support the exchange of medical information objects. All elements of the Participant Model and Communication Model are specified using XML Schema. Core subjects of the Participant Model comprise modelling of medical device-related data, e.g., measurements and settings, alert systems, contextual information (e.g., patient demographics and location information), remote control, and archival information. Model extensibility is provided inherently through the use of XML Schema.textual information like patient demographics and location information, remote control, and archival. Model extensibility is provided inherently through the use of XML Schema. (Additional files are available for this standard at http://standards.ieee.org/downloads/11073/)

eHealth related work has been done in several ETSI Technical Bodies: however, there is currently no specific committee structure for eHealth standardization work. It is felt that the importance of the subject matter could justify the creation of a new ETSI Technical Body, but before taking this step, it is necessary to further analyse the work to be performed. The present document provides the results of an analysis of the applicability of existing ETSI and ETSI/3GPP deliverables for eHealth matters, and specifies the need for further work in this area. Based upon the present document, further actions may be undertaken.

The standard establishes a set of processes by which organizations can include consideration of human ethical values throughout the stages of concept exploration and development. This standard supports management and engineering in transparent communication with selected stakeholders for values elicitation and prioritization. It involves traceability of ethical values through an operational concept, value propositions, and value dispositions in the system design. The standard describes processes that provide for traceability of ethical values in the concept of operations, ethical requirements, and ethical risk-based design. It is applicable for all sizes and types of organizations using their own life cycle models.

ISO 35106:2017 specifies requirements and provides recommendations and guidance for the collection, analysis and presentation of relevant physical environmental data for activities of the petroleum and natural gas industries in arctic and cold regions. Activities include design and operations, which involve planning and actual execution.
Reference to arctic and cold regions in this document is deemed to include both the Arctic and other locations characterized by low ambient temperatures and the presence or possibility of sea ice, icebergs, shelf ice, glaciers, icing conditions, persistent snow cover, frozen surfaces of lakes and rivers, localized and rapidly changing weather systems and/or permafrost.
ISO 35106:2017 outlines requirements for a range of different operations that have been or are presently being undertaken and for existing design concepts. This document can also be used for other operations and new design concepts in arctic and cold regions as long as it is recognized that all data requirements are not necessarily addressed.

This guide provides the technical background, rationale and guidance to support the application of the substantially revised IEEE 1547, Standard for Interconnection and interoperability of Distributed Energy Resources (DER) with Electric Power Systems (EPS) and Associated Interfaces. The document will describe how the requirements and default settings specified in 1547 have been carefully chosen to balance distribution and bulk system needs for increasing penetration of DER. It further expands IEEE 1547 by addressing certain DER integration issues that are not fully addressed by the base standard, e.g. reclosing coordination and limitation of over-voltage in the Area EPS. The guide will address (1) the concept of the newly-introduced performance categories and their assignment to specific DER by an Authority Governing Interconnection Requirements (AGIR); (2) the new requirements for voltage and reactive power control, frequency control, response to abnormal conditions including ride-through; (3) the flexibility provided by the newly-introduced ranges of adjustability for control settings as well as for voltage and frequency trip settings to fully exploit the revised IEEE 1547's potential and to account for specific system characteristics; (4) the interoperability and communication interface requirements; and (5) the test and verification practices, including design and as-built installation evaluations for utility-scale DER, that have not been included in the previous version of the standard. Presented in the document are technical descriptions and schematics, applications guidance and interconnection examples to enhance the use of IEEE 1547.