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
This document is to establish a test method for exoskeleton-type WALKING RACA ROBOT which is intended to move from one location to another, by making reciprocating motion having intermittent contact with the travel surface.
This document provides guidance on safety measures for the design and integration of end-effectors used for robot systems. The integration includes the following:— the manufacturing, design and integration of end-effectors. — the necessary information for use.This document provides additional safety guidance on the integration of robot systems, as described in ISO 10218‑2:2011.
ISO 14539 is one of a series of standards dealing with the requirements of manipulating industrial robots. Other documents cover such topics as terminology, general characteristics, coordinate systems, performance criteria and related test methods, safety, mechanical interfaces and graphical user interfaces for programming
ISO 9409-2:2002 defines the main dimensions, designation and marking for a shaft with cylindrical projection as mechanical interface. It is intended to ensure the exchangeability and to keep the orientation of hand-mounted end effectors.ISO 9409-2:2002 does not contain any correlation of load-carrying ranges.The mechanical interfaces specified in ISO 9409-2:2002 will also find application in simple handling systems which are not covered by the definition of manipulating industrial robots, such as pick-and-place or master-slave units.