SFS Suomen Standardit

 

 

 

 

The purpose of this document is to specify the categorial structure within the subject field of acupuncture by defining a set of domain constraints of sanctioned characteristics each composed of a semantic link and an applicable characterizing category in order to represent the concept of acupuncture point. This document describes sanctioned characteristics with semantic links and characterizing categories for representation of acupuncture points. concepts of Acupuncture points are used in clinical practices for applying stimulation such as insertion, pricking, scratching, scrubbing, massaging or pressing with various kinds of needles, moxibustion, acupressure and cupping in various medical systems.

 

This document defines a cybersecurity labelling framework for the development and implementation of cybersecurity labelling programmes for consumer IoT products. It provides requirements and includes guidance on the following topics: This document is limited to consumer IoT products, such as IoT gateways, base stations and hubs to which multiple devices connect; smart cameras, televisions, and speakers; wearable devices; connected smoke detectors, door locks and window sensors; connected home automation and alarm systems; connected appliances, such as washing machines and fridges; smart home assistants; and connected children’s toys and baby monitors. Products that are not intended for consumer use are excluded from this standard. Examples of excluded devices are those that are primarily intended for manufacturing, healthcare and other industrial purposes. This document is applicable to Consumers, Developers, issuing bodies of cybersecurity labels and Conformity Assessment Bodies.

 

This document provides the specialized requirements to demonstrate competence of individuals in performing IT product security evaluations and certifications in accordance with the ISO/IEC 15408 series and ISO/IEC 18045.

 

This International Standard specifies a method for assessing the heat penetration resistance of materials intended for use in clothing to protect against large splashes of molten metal. It provides specific procedures for assessing the effects of splashes of molten aluminium, molten cryolite, molten copper, molten iron and molten mild steel. The principle of the test method is applicable to a wider range of hot molten materials than those for which specific procedures are set out, provided that appropriate measures are applied to protect the test operator. It is important to note that good resistance of a material to a pure molten metal does not guarantee a good performance against any slag that can be present in a manufacturing process.

 

This document contains simulation software for the MPEG-Immersive Audio standard as defined in ISO/IEC 23090-4.

 

This part of ISO 11843 presents methods for determining the critical value of the response variable and the minimum detectable value in Poisson distribution measurements. It is applicable when variations in both the background noise and the signal are describable by the Poisson distribution. The conventional approximation is used to approximate the Poisson distribution by the normal distribution consistent with ISO 11843-3 and ISO 11843-4. The accuracy of the normal approximation as compared to the exact Poisson distribution is discussed in Annex C.

 

 

This Recommendation | International Standard establishes controls, purpose, and guidance for implementing controls, to meet the requirements identified by a risk and impact assessment related to the protection of personally identifiable information (PII). In particular, this Recommendation | International Standard specifies guidance based on ISO/IEC 27002, taking into consideration the controls for processing PII that may be applicable within the context of an organization's privacy risk environment(s). This Recommendation | International Standard is applicable to all types and sizes of organizations acting as PII controllers (as defined in ISO/IEC 29100), including public and private companies, government entities and not-for-profit organizations that process PII, in particular, organizations that do not establish or operate a privacy information management system.

 

This document describes laboratory test methods to determine the resistance of materials used in protective clothing, including gloves and including footwear, when the footwear is an integral part of the clothing, to permeation by liquid or gaseous chemicals under the conditions of continuous contact. This test method is referred to in ISO 16602-3. Method A is applicable to testing against liquid chemicals, either volatile (with a vapour pressure in excess of 133,332 Pa (1 mmHg) at 20 °C) or sufficiently soluble in water (such that detection limits are possible that allow breakthrough times and/or cumulative permeation parameters to be measured), expected to be in continuous contact with the protective clothing material. Method B is applicable to testing against gaseous chemicals expected to be in continuous contact with the protective clothing material. These test methods assess the permeation resistance of the protective clothing material under laboratory conditions in terms of cumulative permeation, permeation rate and breakthrough time. These test methods also enable qualitative observations to be made of the effects of the test chemical on the material under test. These test methods are only suitable for measuring permeation by liquids and gases. Permeation by solid challenge chemicals is beyond the scope of this document. These test methods address only the performance of materials or certain materials' constructions (e.g. seams). These test methods do not address the design, overall construction and components, or interfaces of garments, or interfaces between garments and gloves or garments and footwear, or other factors which may affect the overall chemical protection offered by protective clothing, gloves or footwear or combinations of chemical protective clothing, gloves and footwear. It is emphasized that these tests do not necessarily simulate conditions to which materials are likely to be exposed in practice. In most cases the conditions of the permeation test will be far more challenging than expected workplace conditions.

 

This document provides guidelines on using zero-knowledge proofs (ZKP) to improve privacy by reducing the risks associated with the sharing or transmission of personal data between organisations and users by minimizing unnecessary information disclosure. It includes several ZKP functional requirements relevant to a range of different business use cases, then describes how different ZKP models can be used to meet those functional requirements securely.

 

This part of ISO 17090 specifies the certificate profiles required to interchange healthcare information within a single organization, between different organizations and across jurisdictional boundaries. It details the use made of digital certificates in the health industry and focuses, in particular, on specific healthcare issues relating to certificate profiles.

 

 

This document defines the basic concepts underlying the use of digital certificates in healthcare and provides a scheme of interoperability requirements to establish a digital certificate-enabled secure communication of health information. It also identifies the major stakeholders who are communicating health-related information, as well as the main security services required for health communication where digital certificates can be required. This document gives a brief introduction to public key cryptography and the basic components needed to deploy digital certificates in healthcare. It further introduces different types of digital certificates — identity certificates and associated attribute certificates for relying parties, self-signed certification authority (CA) certificates, and CA hierarchies and bridging structures.

 

 

This document gives guidelines for certificate management issues involved in deploying digital certificates in healthcare. It specifies a structure and minimum requirements for certificate policies, as well as a structure for associated certification practice statements. This document also identifies the principles needed in a healthcare security policy for cross-border communication and defines the minimum levels of security required, concentrating on aspects unique to healthcare.

 

 

This part of ISO 17090 supports interchangeability of digital signatures and the prevention of incorrect or illegal digital signatures by providing minimum requirements and formats for generating and verifying digital signatures and related certificates. Furthermore, it defines the provable compliance with a PKI policy necessary in the domain of healthcare. This part of ISO 17090 adopts long-term signature formats to ensure integrity and non-repudiation in long-term electronic preservation of healthcare information. The part of ISO 17090 conforms to ISO/ETSI standards for long-term signature formats to improve and guarantee interoperability in the healthcare field. There is no limitation regarding the data format and the subject for which the signature is created.

 

 

This Technical Specification indicates the data elements and structure suited to accurate and procedurally appropriate and sensitive identification of individuals in health care in a face-to-face setting supported by computer technology, or through interactions between computer systems. It provides guidelines for improving the positive identification of subjects of care within and between health care organizations. It defines demographic and other identifying data elements suited to capturing subject of care identification in health care settings, and the wide variety of manual and computer enhanced procedures used for this process. It provides guidance on the application of these procedures in the manual and the computer environment and makes recommendations about the nature and form of health care identifiers, the management organization to oversee subject of care identification and computer support to be provided for the identification process. There are additional factors to be considered in providing access to distributed subject of care data, including privacy, security and data transfer mechanisms; these are outside the scope of this Technical Specification. Application of this Technical Specification will increase the capacity for data access. Authorization of such access is determined by the application of legislation, organizational policies and guidelines, and professional ethics.

 

 

The Health Level Seven (HL7) Reference Information Model (RIM) is a static model of health and health care information as viewed within the scope of HL7 standards development activities. It is the combined consensus view of information from the perspective of the HL7 working group and the HL7 international affiliates. The RIM is the ultimate source from which all HL7 version 3.0 protocol specification standards draw their information-related content. In the context of ISO TC215 – Health Informatics, the RIM provides a reference model that has been and will likely continue to be used in developing further health informatics specifications.