ISO

Specifies general definitions for low-speed serial data communication up to 125 kbit/s for road vehicle applications. The object is to define the general architecture of the communication network and the content of the data link layer and the physical layer for transmission between the different types of electronic modules on board road vehicles. Parts 2, 3 and 4 are entirely independent.

ISO 24100:2010, 3.3. Intelligent transport systems::Basic principles for personal data protection in probe vehicle information services

ISO/TR 17427-9:2015, 2.5.Intelligent transport systems::Cooperative ITS::Part 9: Compliance and enforcement aspects

ISO/TS 17975:2015, 3.1. Health informatics::Principles and data requirements for consent in the Collection, Use or Disclosure of personal health information

ISO/TS 21089:2018 describes trusted end-to-end flow for health information and health data/record management. Health data is originated and retained, typically as discrete record entries within a trusted electronic health record (EHR), personal health record (PHR) or other system/device. Health data can include clinical genomics information.Health record entries have a lifespan (period of time managed by one or more systems) and within that lifespan, various lifecycle events starting with (1) originate/retain. Subsequent record lifecycle events may include (2) update (3) attest (4) disclose (5) transmit (6) receive (7) access/view, and more. A record entry instance is managed over its lifespan by the source system. If record entry content is exchanged, this instance may also be managed intact by one or more downstream systems. Consistent, trusted management of record entry instances is the objective of this document, continuously and consistently whether the instance is at rest or in motion, before/during/after each lifecycle event, across one or more systems.

This document specifies a generic business process framework for a smart city focusing solely on smart city-specific processes. Generic business processes common between smart cities and commercial organizations are be identified but not detailed.

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

ISO 25237:2017 contains principles and requirements for privacy protection using pseudonymization services for the protection of personal health information. This document is applicable to organizations who wish to undertake pseudonymization processes for themselves or to organizations who make a claim of trustworthiness for operations engaged in pseudonymization services. It (a) defines one basic concept for pseudonymization, (b) defines one basic methodology for pseudonymization services including organizational, as well as technical aspects, (c) specifies a policy framework and minimal requirements for controlled re-identification,(d) gives an overview of different use cases for pseudonymization that can be both reversible and irreversible,(e) gives a guide to risk assessment for re-identification, (f) provides an example of a system that uses de-identification, (g) provides informative requirements to an interoperability to pseudonymization services, and (h) specifies a policy framework and minimal requirements for trustworthy practices for the operations of a pseudonymization service

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

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/TS 14265:2011, 2.9.Health Informatics - Classification of purposes for processing personal health information

ISO 10218-2:2011 specifies safety requirements for the integration of industrial robots and industrial robot systems as defined in ISO 10218-1, and industrial robot cell(s). The integration includes the following:the design, manufacturing, installation, operation, maintenance and decommissioning of the industrial robot system or cell. necessary information for the design, manufacturing, installation, operation, maintenance and decommissioning of the industrial robot system or cell. component devices of the industrial robot system or cell.ISO 10218-2:2011 describes the basic hazards and hazardous situations identified with these systems, and provides requirements to eliminate or adequately reduce the risks associated with these hazards. ISO 10218-2:2011 also specifies requirements for the industrial robot system as part of an integrated manufacturing system. ISO 10218-2:2011 does not deal specifically with hazards associated with processes (e.g. laser radiation, ejected chips, welding smoke). Other standards can be applicable to these process hazards.