SFS Suomen Standardit

 

The scope of EN 203 1:2021+A1:2023 applies, with the following modifications: - replace the 2nd paragraph with the following: This document applies to brat pans.

 

The scope of EN 203-1:2021+A1:2023 applies, with the following modifications: - replace the 2nd paragraph with the following: This document applies to gas heated boiling pans and pasta cookers.

 

This document specifies requirements, test methods, marking and manufacturer’s instructions and information for descender devices fitted with a built-in speed-regulating system, which include descent lines (hereinafter referred to as lines). These descender devices are intended to be used in a rescue system to provide protection against falling from a height when accessing/leaving positions at a height. This document does not specify requirements for descender devices that are used for descending in mountaineering, rope access or work positioning systems.

 

This document specifies the requirements and describes the methods for design, installation, testing and maintenance of low, medium, and high expansion foam fire extinguishing systems. Foam systems may be used to suppress the release of toxic vapours but this application is outside the scope of this document. This document provides guidance for the design of various foam systems available to persons with knowledge and experience in determining the selection of foam fire extinguishing systems which will be effective in protecting specific hazard configurations. For the application of this standard, a risk assessment by a qualified and experienced person should be performed for both new and existing systems, however the risk assessment is outside the scope of this document. This document does not cover a risk analysis carried out by a competent person. Nothing in this document is intended to restrict new technologies or alternative arrangements, provided that the level of foam system performance prescribed in this standard is not lowered, and supported by documented evidence/test reports. All foam systems are generally unsuitable for the following: - chemicals, such as cellulose nitrate, that release sufficient oxygen or other oxidizing agents which can sustain combustion; - energized unenclosed electrical equipment; - metals such as sodium, potassium and sodium-potassium alloys which are reactive to water; - hazardous, water-reactive materials such as triethyl-aluminium and phosphorous pentoxide; - combustible metals such as aluminium and magnesium.

 

This document specifies the following for raw bovine hides and skins intended for use throughout the leather manufacturing supply chain: - Terms and definitions; - Rules for the presentation of raw hides and skins. It applies to fresh and salted bovine hides and skins. It is not the aim of this document to interfere with the normal commercial agreement between the buyer and the supplier of hides and skins, on the contrary, it should be able to be used as a basis. This document is intended to avoid disagreements between parties. It is the result of discussions with representatives of agriculture, slaughterhouses, skin trade and tanneries. It shows which parts of hides and skins can be used for leather production and which factors influence the quality of hides and skins. Furthermore, it gives recommendations on precautions to be taken for transport, preservation, loading and unloading, selection of tanned hides, classification of hides, weight, loss and tax exemption, identification of hides.

 

 

This document gives guidelines to select the test methods to assess the performance of leather for automotive. This document also specifies the sampling and conditioning procedures of specimens. NOTE Regulations on chemical substances in consumer goods might differ from country to country requiring for any given market a special attention to restricted substances.

 

This document provides requirements and guidelines for the application of the book and claim chain of custody model. It is applicable to any flow of materials or products or processes within a system, including how to attribute specified characteristics to flows of such processes. This document provides requirements and guidelines for the following matters, amongst others:

 

This document provides requirements and guidelines for the application of the mass balance chain of custody model, as defined in ISO 22095, to any material or product flow within mass balance systems, including how to attribute specified characteristics to flows of such processes. This document provides requirements and guidelines for the following matters, amongst others:

 

 

ISO 27799:2016 gives guidelines for organizational information security standards and information security management practices including the selection, implementation and management of controls taking into consideration the organization's information security risk environment(s). It defines guidelines to support the interpretation and implementation in health informatics of ISO/IEC 27002 and is a companion to that International Standard. ISO 27799:2016 provides implementation guidance for the controls described in ISO/IEC 27002 and supplements them where necessary, so that they can be effectively used for managing health information security. By implementing ISO 27799:2016, healthcare organizations and other custodians of health information will be able to ensure a minimum requisite level of security that is appropriate to their organization's circumstances and that will maintain the confidentiality, integrity and availability of personal health information in their care. It applies to health information in all its aspects, whatever form the information takes (words and numbers, sound recordings, drawings, video, and medical images), whatever means are used to store it (printing or writing on paper or storage electronically), and whatever means are used to transmit it (by hand, through fax, over computer networks, or by post), as the information is always be appropriately protected. ISO 27799:2016 and ISO/IEC 27002 taken together define what is required in terms of information security in healthcare, they do not define how these requirements are to be met. That is to say, to the fullest extent possible, ISO 27799:2016 is technology-neutral. Neutrality with respect to implementing technologies is an important feature. Security technology is still undergoing rapid development and the pace of that change is now measured in months rather than years. By contrast, while subject to periodic review, International Standards are expected on the whole to remain valid for years. Just as importantly, technological neutrality leaves vendors and service providers free to suggest new or developing technologies that meet the necessary requirements that ISO 27799:2016 describes. As noted in the introduction, familiarity with ISO/IEC 27002 is indispensable to an understanding of ISO 27799:2016. The following areas of information security are outside the scope of ISO 27799:2016: a) methodologies and statistical tests for effective anonymization of personal health information; b) methodologies for pseudonymization of personal health information (see Bibliography for a brief description of a Technical Specification that deals specifically with this topic); c) network quality of service and methods for measuring availability of networks used for health informatics; d) data quality (as distinct from data integrity).

 

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This document provides a set of information security controls, including implementation guidance, for health organizations. It is based on ISO/IEC 27002:2022. In addition to generic ICT equipment and software used in many other environments, the scope of this document includes software and systems specifically for healthcare, such as electronic health record systems and medical devices incorporating health software. Such medical devices can be programmed or programmable and can contain software, firmware or both. Also in scope is other digital equipment (such as that for environmental and infection control, building management, and physical security) that can be used in premises where healthcare is provided. This document applies to health and other relevant information in all its aspects, whatever form the information takes (including text and numbers, sound recordings, drawings, images and video), by whatever means it has been acquired or captured, whatever means are used to store it (such as printing or writing on paper or storage electronically), and whatever means are used to transfer or exchange it (orally, by hand, by post, movement of storage media, direct links or networking). This document is for organizations of all types and sizes that provide healthcare or are custodians of personal health information for other reasons. The information that they are responsible for can be stored and processed in many possible ways and locations, including on premises or in the cloud, but remains in scope. This document applies to all physical settings where healthcare is intended to be delivered, such as hospitals, clinics and other locations or facilities designated for healthcare purposes such as ambulances and mobile imaging or diagnostic units. It also applies to care provided elsewhere, such as in residential premises. In addition to the range of settings, this document applies to all methods of service provision including remote or virtual healthcare.

 

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— yhdenmukaistaminen ISO/IEC 27002:2022 -standardin uuden rakenteen ja siihen tehtyjen muutosten kanssa verrattuna edelliseen versioon
— terveydenhuoltoon liittyvien hallintakeinojen tarkistus ja lisäys
— sellaisten sisältöjen poistaminen, jotka sisältyvät ISO/IEC 27002:2022 -standardiin, mutta eivät olleet sen aiemmassa versiossa
— informatiivisten liitteiden lisääminen, jotka sisältävät

 

This Recommendation | International Standard gives guidelines for information security controls applicable to the provision and use of cloud services by providing: This Recommendation | International Standard provides controls and guidance for CSCs and CSPs. This Recommendation | International Standard excludes any and all aspects of conformity assessment.

 

This document specifies a framework for representing data recorded in terminological data collections (TDCs). This framework includes a metamodel and methods for describing specific terminological markup languages (TMLs), exemplified in this document in eXtensible Markup Language (XML). The mechanisms for implementing constraints in a TML are defined, but not the specific constraints for individual TMLs. This document is designed to support the development and use of computer applications for terminological data and the exchange of such data between different applications. This document also defines the conditions that allow the data expressed in one TML to be mapped onto another TML.

 

 

This document specifies an ageing method for phosphate ester turbine control fluids. These products fall into category HFDR of ISO 6743-4[1] and into categories TSD, TGD and TCD of ISO 6743-5.[2] The amount of acid developed during the test are used to assess the level of anti-aging performance. The standard includes apparatus, reagents & materials, sampling, preparations, test methods, calculation, reports etc. This document is applicable to anti-ageing performance determination for phosphate ester turbine control fluids both new and in-service. This document does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

 

ISO/IEC 17020:2012 specifies requirements for the competence of bodies performing inspection and for the impartiality and consistency of their inspection activities. It applies to inspection bodies of type A, B or C, as defined in ISO/IEC 17020:2012, and it applies to any stage of inspection.

 

This document specifies three methods for quantitative measurement of crystalline silica (CS) major polymorphs (quartz and cristobalite) weight percentage content in bulk samples using XRPD. General information is provided about their capabilities and limitations of relevance to laboratories working for routine testing. Only X-ray diffractometers with Bragg-Brentano geometry are considered. The analysed specimen should be in the form of loose powder, where the median grain size is between 1 and 10 µm physical diameter. Block specimens are not considered. Although a number of methods of analysis are considered in this document, other XRPD methods of analysis could be considered if demonstrated to give equivalent results.