Allmänt. Terminologi. Standardisering. Dokumentation

This document provides guidance based on ISO/IEC 27002:2013 applied to process control systems used by the energy utility industry for controlling and monitoring the production or generation, transmission, storage and distribution of electric power, gas, oil and heat, and for the control of associated supporting processes. This includes in particular the following:

— central and distributed process control, monitoring and automation technology as well as information systems used for their operation, such as programming and parameterization devices;

— digital controllers and automation components such as control and field devices or Programmable Logic Controllers (PLCs), including digital sensor and actuator elements;

— all further supporting information systems used in the process control domain, e.g. for supplementary data visualization tasks and for controlling, monitoring, data archiving, historian logging, reporting and documentation purposes;

— communication technology used in the process control domain, e.g. networks, telemetry, telecontrol applications and remote control technology;

— Advanced Metering Infrastructure (AMI) components, e.g. smart meters;

— measurement devices, e.g. for emission values;

— digital protection and safety systems, e.g. protection relays, safety PLCs, emergency governor mechanisms;

— energy management systems, e.g. of Distributed Energy Resources (DER), electric charging infrastructures, in private households, residential buildings or industrial customer installations;

— distributed components of smart grid environments, e.g. in energy grids, in private households, residential buildings or industrial customer installations;

— all software, firmware and applications installed on above-mentioned systems, e.g. DMS (Distribution Management System) applications or OMS (Outage Management System);

— any premises housing the above-mentioned equipment and systems;

— remote maintenance systems for above-mentioned systems.

This document does not apply to the process control domain of nuclear facilities. This domain is covered by IEC 62645.

This document also includes a requirement to adapt the risk assessment and treatment processes described in ISO/IEC 27001:2013 to the energy utility industry-sector–specific guidance provided in this document.

This document prescribes safety signs for the purposes of accident prevention, fire protection, health hazard information and emergency evacuation.

The shape and colour of each safety sign are according to ISO 3864-1 and the design of the graphical symbols is according to ISO 3864-3.

This document is applicable to all locations where safety issues related to people need to be addressed. However, it is not applicable to the signalling used for guiding rail, road, river, maritime and air traffic and, in general, to those sectors subject to a regulation which may differ with regard to certain points of this document and of the ISO 3864 series.

This document specifies the safety sign originals that can be scaled for reproduction and application purposes.

This International document establishes requirements for healthcare interpreting services in spoken and signed communication. Healthcare interpreting services: a) enable safe communication mainly between healthcare providers and patients b) provide linguistic access to healthcare services, and c) ensure patient safety. This International document is applicable to all situations requiring healthcare interpreting, where the parties involved need to communicate orally, or by signed language, to resolve a health-related issue. It covers all parties involved in facilitating communication in healthcare settings. However, it does not supersede national, state or provincial regimes or legislation, which govern interpreting services in healthcare, where applicable.

The objectives of this document are: a) to establish minimum requirements; b) to promote market transparency in the field of healthcare interpreting; c) to provide information and clarification for users of healthcare interpreting services.

This document is aimed at individuals, the users of these services and all parties involved in the work of healthcare interpreting:

— Healthcare interpreters

— Interpreting service providers

— Patients and accompanying persons

— In-house interpreter departments

— Government agencies

— Non-profit organizations

— Community organizations that provide interpreting services

— Employees that provide interpreting services

— Professional associations

— Healthcare organizations

— Educators and researchers

— Healthcare providers and staff

— Healthcare policy writers

This International Standard establishes a vocabulary of terms used for anaesthetic and respiratory equipment and supplies, related devices and supply systems.

Note 1 to entry This International Standard is based on standards and drafts which have been produced by ISO/TC 121 and CEN/TC 215.

Note 2 to entry Contrary to the policy in ISO 4135 3rd edition of allowing multiple definitions of the same term in different categories, this document attempts to ensure consistency by the inclusion of a ‘general’ category, and by use of domain specifiers and unique pre-coordinated domain-specific term names.

Note 3 to entry In addition to terms and definitions used in two of the three official ISO languages (English and French), this International Standard gives the equivalent terms in the German language; these are published under the responsibility of the member body for Germany. However, only the terms and definitions given in the official languages can be considered as ISO terms and definitions.

This standard defines terms relevant to automatic end effector exchange systems used in combination with industrial robots as defined in 10218-1:2006 and as parts of robot systems as defined in 10218-2:2006.

The terms are presented by their symbol, unit, definition and description. The definition includes applicable references to existing standards.

Annex A provides Examples of useful technical data of automatic end effector exchange systems.

This document is applicable to papers and boards used for conservation of cellulose based documents.

The scope of this project is to define a general object-oriented information model that may be used to structure information and identify services used in point-of-care (POC) medical device communications. The scope is primarily focused on acute care medical devices and the communication of patient vital signs information.

This document provides a classification and defines terms for absorbent incontinence products.

The document builds on ISO 9999, Assistive products for persons with disability — Classification and terminology, sub-class 09 30 – Absorbing products to contain urine and faeces. This document also provides preferred terms, additional terms and example pictures.

This document specifies the recommended proportions for the symbols used on technical product documentation. It gives recommended dimensions based on the grid related to the line width to be used.

This standard does not apply to symbols used in process plant documentation which is covered in ISO 81714-1.

The proportions of the symbols are based on the standard heights of lettering given in IS0 3098-l.

This document establishes commonly accepted control objectives, controls and guidelines for implementing measures to protect Personally Identifiable Information (PII) in line with the privacy principles in ISO/IEC 29100 for the public cloud computing environment.

In particular, this document specifies guidelines based on ISO/IEC 27002, taking into consideration the regulatory requirements for the protection of PII which can be applicable within the context of the information security risk environment(s) of a provider of public cloud services.

This document is applicable to all types and sizes of organizations, including public and private companies, government entities and not-for-profit organizations, which provide information processing services as PII processors via cloud computing under contract to other organizations.

The guidelines in this document can also be relevant to organizations acting as PII controllers. However, PII controllers can be subject to additional PII protection legislation, regulations and obligations, not applying to PII processors. This document is not intended to cover such additional obligations.

This International Standard gives guidelines for how to process and resolve potential vulnerability information in a product or online service.

This International Standard is applicable to vendors involved in handling vulnerabilities.