This document specifies requirements and provides guidance for bodies providing audit and certification of a privacy information management system (PIMS) according to ISO/IEC 27701, in addition to the requirements contained within ISO/IEC 17021-1.
The requirements contained in this document are demonstrated in terms of competence and reliability by bodies providing PIMS certification. The guidance contained in this document provides additional interpretation of these requirements for bodies providing PIMS certification.
NOTE       This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies requirements and provides guidance for bodies providing audit and certification of a privacy information management system (PIMS) according to ISO/IEC 27701, in addition to the requirements contained within ISO/IEC 17021-1.
The requirements contained in this document are demonstrated in terms of competence and reliability by bodies providing PIMS certification. The guidance contained in this document provides additional interpretation of these requirements for bodies providing PIMS certification.
NOTE       This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies requirements and provides guidance for bodies providing audit and certification of a privacy information management system (PIMS) according to ISO/IEC 27701, in addition to the requirements contained within ISO/IEC 17021-1. The requirements contained in this document are demonstrated in terms of competence and reliability by bodies providing PIMS certification. The guidance contained in this document provides additional interpretation of these requirements for bodies providing PIMS certification. NOTE This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies additional requirements to ISO/IEC 17021-1. The requirements contained in this document, when implemented, support the demonstration of competence, consistency and reliability by the bodies performing auditing and certification of an artificial intelligence management system (AIMS) according to ISO/IEC 42001 for organizations that provide, develop or use AI systems. Certification of AIMS is a third-party conformity assessment activity (as described in ISO/IEC 17000:2020, 4.5), and bodies performing this activity are third-party conformity assessment bodies. This document also provides the necessary information and confidence to customers about the way certification has been granted. NOTE This document can be used as a criteria document for accreditation or peer assessment.

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This TS provides requirements and ISO/IEC 17065 interpretations for Conformity Assessment Bodies (CABs) assessing Cloud Services
This TS is intended to be used by the National Accreditation Bodies (NABs), as well as CABs.

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This TS provides requirements and ISO/IEC 17065 interpretations for Conformity Assessment Bodies (CABs) assessing Cloud Services
This TS is intended to be used by the National Accreditation Bodies (NABs), as well as CABs.

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This document sets out a review of the current methods and practices (including tools, assets, and conditions of acceptability) for
conformity assessment in respect to, among others, products, services, processes, management systems, organizations, or persons,
as relevant for the development and use of AI systems. It includes an industry horizontal (vertical agnostic) perspective as well as an
industry vertical perspective.
This document focuses only on the process of assessment and gap analysis of conformity. It defines the objects of conformity
related to AI systems and all other related aspects of the process of conformity assessment. The document also reviews to what
extent AI poses specific challenges with respect to assessment of, for example, software engineering, data quality and engineering
processes.
This document takes into account requirements and orientations from policy frameworks such as the EU AI strategy and those from
CEN and CENELEC member countries.
This document is intended for technologists, standards bodies, regulators and interested parties.

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This document defines a CCSDS Recommended Practice (and ISO standard) on which to base the operations of the organization(s) which assess the trustworthiness of digital repositories using the latest version of CCSDS 652.0/ISO 16363 (reference REF R_652x0m2AuditandCertificationofTrustwor \h[1] 08D0C9EA79F9BACE118C8200AA004BA90B02000000080000002900000052005F00360035003200780030006D0032004100750064006900740061006E006400430065007200740069006600690063006100740069006F006E006F0066005400720075007300740077006F0072000000 ) and provide the appropriate certification. This document specifies requirements for bodies providing audit and certification of digital repositories, based on the metrics contained within ISO/IEC 17021-1 (reference REF R_ISOIEC170212011ConformityAssessmentReq \h \* MERGEFORMAT [4] 08D0C9EA79F9BACE118C8200AA004BA90B02000000080000002900000052005F00490053004F0049004500430031003700300032003100320030003100310043006F006E0066006F0072006D006900740079004100730073006500730073006D0065006E0074005200650071000000 ) and reference REF R_652x0m2AuditandCertificationofTrustwor \h[1] 08D0C9EA79F9BACE118C8200AA004BA90B02000000080000002900000052005F00360035003200780030006D0032004100750064006900740061006E006400430065007200740069006600690063006100740069006F006E006F0066005400720075007300740077006F0072000000 . It is primarily intended to support the accreditation of bodies providing such certification. ISO/IEC 17021-1 provides the bulk of the requirements on bodies offering audit and certification for general types of management systems. However, for each specific type of system, specific additional requirements will be needed, for example, to specify the standard against which the audit is to be made and the qualifications which auditors require. This document provides the (small number of) specific additions required for bodies providing audit and certification of candidate trustworthy digital repositories. Trustworthy here means that they can be trusted to maintain, over the long-term, the understandability and usability of digitally encoded information placed into their safekeeping. In order improve readability the section numbers are kept consistent with those of ISO/IEC 17021-1. Some subsections are applicable as they stand, and these are simply enumerated; otherwise additions to subsections are explicitly given. In the former case the sections may consist of just a few sentences. As a result this document must be read in conjunction with ISO/IEC 17021-1. The requirements contained in this CCSDS Recommended Practice need to be demonstrated in terms of competence and reliability by any organization or body providing certification of digital repositories.

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This document sets out a review of the current methods and practices (including tools, assets, and conditions of acceptability) for
conformity assessment in respect to, among others, products, services, processes, management systems, organizations, or persons,
as relevant for the development and use of AI systems. It includes an industry horizontal (vertical agnostic) perspective as well as an
industry vertical perspective.
This document focuses only on the process of assessment and gap analysis of conformity. It defines the objects of conformity
related to AI systems and all other related aspects of the process of conformity assessment. The document also reviews to what
extent AI poses specific challenges with respect to assessment of, for example, software engineering, data quality and engineering
processes.
This document takes into account requirements and orientations from policy frameworks such as the EU AI strategy and those from
CEN and CENELEC member countries.
This document is intended for technologists, standards bodies, regulators and interested parties.

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This document provides guidance to validation/verification programme owners, validation/verification bodies and interested parties on the development, content and operation of validation/verification programmes.
When implemented by validation/verification bodies, this document is intended to be used in conjunction with ISO/IEC 17029 and sector-specific applications of ISO/IEC 17029.

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  • Technical specification
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This New Work Item Proposal has the scope to provide an amendment of the European standard EN 50463-5 in order to update the annex ZZ

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This document provides guidance to validation/verification programme owners, validation/verification bodies and interested parties on the development, content and operation of validation/verification programmes. When implemented by validation/verification bodies, this document is intended to be used in conjunction with ISO/IEC 17029 and sector-specific applications of ISO/IEC 17029.

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  • Technical specification
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This document provides guidance on the use of remote auditing methods in auditing management systems. It is applicable to all organizations that plan and conduct all kinds of internal or external audits (i.e. first-party, second-party and third-party audits) of management systems.
This document supports the general principles of auditing given in ISO 19011:2018 and provides further guidance on specific conditions, possibilities and limitations for implementing remote auditing methods.
This document is intended to strengthen confidence in the use of remote auditing methods for auditing management systems among customers, regulators, accreditation bodies, certification bodies, scheme owners, industry, employees, consumers, suppliers and other interested parties.
The use of remote auditing methods for auditing management systems is not intended to replace on-site audit methods. Instead, remote auditing methods are intended to serve as a tool to effectively and efficiently conduct the audit.
NOTE This document can be used for other types of audits and assessments.

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  • Technical specification
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  • Technical specification
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This document provides guidance on the use of remote auditing methods in auditing management systems. It is applicable to all organizations that plan and conduct all kinds of internal or external audits (i.e. first-party, second-party and third-party audits) of management systems. This document supports the general principles of auditing given in ISO 19011:2018 and provides further guidance on specific conditions, possibilities and limitations for implementing remote auditing methods. This document is intended to strengthen confidence in the use of remote auditing methods for auditing management systems among customers, regulators, accreditation bodies, certification bodies, scheme owners, industry, employees, consumers, suppliers and other interested parties. The use of remote auditing methods for auditing management systems is not intended to replace on-site audit methods. Instead, remote auditing methods are intended to serve as a tool to effectively and efficiently conduct the audit. NOTE This document can be used for other types of audits and assessments.

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This document specifies prerequisite requirements for application for the certification of new lifts (elevators), model lifts, lift components and lift functions. NOTE Hereinafter in this document, the term “lift” is used instead of the term “elevator”.

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This document specifies requirements for conformity assessment bodies (CABs) performing certification of new lifts (elevators), model lifts, lift components and lift functions. NOTE Hereinafter in this document, the term “lift” is used instead of the term “elevator”.

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This document provides the solution for auditors to obtain the regulated financial report data and the payroll data. This document is applicable for government audits, as well as external independent audits and internal audits.

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This document complements the existing requirements of ISO/IEC 17021-1 for bodies providing audit and certification of quality management systems against ISO 19443.
NOTE          This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies the functional requirements that build on ISO 21378 for audits in the areas of customs duties and indirect taxes [e.g. value-added tax (VAT) and excise duties]. It addresses how tax auditors obtain audit data for these audits, including data element formats and to some extent content requirements. In practice, this document applies to virtually every step in the whole process in the supply chain and covers both goods, services and works. It includes domestic transactions, cross-border transactions (import and export) and can cover both third-party and intercompany transactions or even movements of goods within the same company. This document does not describe when an event is taxable nor how to calculate tax or customs duties as this is legislation-specific and the situation can vary from country to country or even within the same country. This document covers standard exchange of the data related to taxable operations/activities by businesses to perform controls and audits more effectively and efficiently through automated tests. This document focuses on the characteristics related to taxability and the related formalities of the indirect tax and customs duties regulations. It includes the result of a tax calculation, the relevant underlying parameters which can be processed by ERP-systems and/or indirect tax/customs duties systems, and data needed to comply with indirect tax and customs duties legislation and formalities. This document is not designed to collect audit data from the regulators like tax and/or customs authorities.

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This document specifies requirements and provides guidance for bodies providing audit and certification of an information security management system (ISMS), in addition to the requirements contained within ISO/IEC 17021-1.
The requirements contained in this document are demonstrated in terms of competence and reliability by bodies providing ISMS certification. The guidance contained in this document provides additional interpretation of these requirements for bodies providing ISMS certification.
NOTE       This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document complements the existing requirements of ISO/IEC 17021-1 for bodies providing audit and certification of quality management systems against ISO 19443.
NOTE          This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document complements the existing requirements of ISO/IEC 17021-1 for bodies providing audit and certification of quality management systems against ISO 19443. NOTE This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies requirements and provides guidance for bodies providing audit and certification of an information security management system (ISMS), in addition to the requirements contained within ISO/IEC 17021-1.
The requirements contained in this document are demonstrated in terms of competence and reliability by bodies providing ISMS certification. The guidance contained in this document provides additional interpretation of these requirements for bodies providing ISMS certification.
NOTE       This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies requirements and provides guidance for bodies providing audit and certification of an information security management system (ISMS), in addition to the requirements contained within ISO/IEC 17021-1. The requirements contained in this document are demonstrated in terms of competence and reliability by bodies providing ISMS certification. The guidance contained in this document provides additional interpretation of these requirements for bodies providing ISMS certification. NOTE This document can be used as a criteria document for accreditation, peer assessment or other audit processes.

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This document specifies baseline requirements for demonstrating processing activities compliance with the European personal data protection normative framework in accordance with EN ISO/IEC 17065. It does not however apply to products or management systems destined for processing personal data.
This document is applicable to all organizations which, as personal data controllers and/or processors, process personal data, and its objective is to provide a set of requirements enabling such organizations to conform effectively with the European personal data protection normative framework.
An organization can decide that the standard is applicable only to a specific subset of its processing activities if such a decision does not involve failure to conform with the European personal data protection normative framework.
This document also provides indications for conformity assessment with the aforementioned requirements.

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This document provides specifications for a transport format which enables the digital encapsulation of this data. This document refers to an encapsulation of hardware identification (HWID) data as a HWID tag, just as ISO/IEC 19770-2 refers to software identification (SWID) tags for software identification. This document applies to the following. — Tag producers: organizations that create HWID tags for use by others in the market. A tag producer can be part of the organization creating the hardware or a third-party organization. These organizations can be broken down into two major categories. — Device or component providers: entities responsible for the manufacturing or creation of the hardware device and/or associated operating system, virtual environment, or application platform. Platform providers which support this document can additionally provide tag management capabilities at the level of the platform or operating system. — Tag tool providers: entities that provide tools to create hardware identification tags. For example, tools within development environments that generate hardware identification tags, or installation tools that can create tags on behalf of the installation process, and/or desktop management tools that can create tags for underlying hardware, virtual machines, or platforms that did not originally have a hardware identification tag. — Tag consumers: tools and/or organizations who utilize information from HWID tags are broken down into the following two major categories. — Device or component consumers: entities that purchase, install, integrate, and/or otherwise deploy physical or virtual hardware or components. — IT discovery and processing tool providers: entities that provide tools to collect, store, and process hardware identification tags. These tools may be targeted at a variety of different market segments, including security, asset management, and logistics. This document deals only with hardware device or component identification. This document does not detail information technology asset management (ITAM) processes required for discovery and management of hardware (which is provided in ISO/IEC 19770-1) software identification tags (as defined by ISO/IEC 19770-2), entitlement tags (as defined by ISO/IEC 19770-3), or resource utilization measurements (as defined by ISO/IEC 19770-4).

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This document specifies the performance criteria and test procedures for the performance test of stationary automated measuring systems (AMS) that continuously measure gases and particulate matter in, and flow of, the waste gas from stationary sources.
This document supports the requirements of particular EU Directives. It provides the detailed procedures covering the QAL1 requirements of EN 14181 and, where required, input data used in QAL3.

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This document provides a harmonized process and documentation requirements for the establishment of CoCs used to attest the conformity of aviation, space, and defence products (e.g. assemblies, sub-assemblies, equipment and systems, parts, material, software) or services. It includes a CoC template and supporting instructions on how to complete it.
When quoted by the customer in a contractual requirement, application of this document is mandatory. In other cases, its use is recommended, but if there is a conflict between the requirements of this document and customer or applicable statutory/regulatory requirements, the latter take precedence.
This document can be used by other industries that require the use/application of a CoC.
Requirements for the establishment of Authorized Release Certificates (ARCs) [e.g. European Union Aviation Safety Agency (EASA) Form 1, Federal Aviation Administration (FAA) 8130-3 tag, Civil Aviation Administration of China (CAAC) Form 038] by an external provider holding a production approval (for new aviation products, production, or spares) or maintenance approval (i.e. for in service repairs, modifications, after sales maintenance, overhaul activities, inspections) are not covered by this document, as applicable rules are defined by the aviation authorities having granted these approvals.

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This document defines the industry-accepted requirements for the ICOP scheme, which provides confidence to ASD customers, that organizations with certification of their QMS, issued by accredited CBs, meet applicable AQMS standard requirements. The requirements in this document are applicable to all participants in the ICOP scheme. If there is a conflict between the requirements of this document, and customer or applicable statutory/regulatory requirements, the latter takes precedence.

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This document provides a harmonized process and documentation requirements for the establishment of CoCs used to attest the conformity of aviation, space, and defence products (e.g. assemblies, sub-assemblies, equipment and systems, parts, material, software) or services. It includes a CoC template and supporting instructions on how to complete it.
When quoted by the customer in a contractual requirement, application of this document is mandatory. In other cases, its use is recommended, but if there is a conflict between the requirements of this document and customer or applicable statutory/regulatory requirements, the latter take precedence.
This document can be used by other industries that require the use/application of a CoC.
Requirements for the establishment of Authorized Release Certificates (ARCs) [e.g. European Union Aviation Safety Agency (EASA) Form 1, Federal Aviation Administration (FAA) 8130-3 tag, Civil Aviation Administration of China (CAAC) Form 038] by an external provider holding a production approval (for new aviation products, production, or spares) or maintenance approval (i.e. for in service repairs, modifications, after sales maintenance, overhaul activities, inspections) are not covered by this document, as applicable rules are defined by the aviation authorities having granted these approvals.

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This document specifies competence requirements for personnel involved in the audit and certification process for management systems for quality in healthcare organizations. It complements the existing requirements of ISO/IEC 17021-1.

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This document defines the industry-accepted requirements for the ICOP scheme, which provides confidence to ASD customers, that organizations with certification of their QMS, issued by accredited CBs, meet applicable AQMS standard requirements. The requirements in this document are applicable to all participants in the ICOP scheme. If there is a conflict between the requirements of this document, and customer or applicable statutory/regulatory requirements, the latter takes precedence.

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This document defines the rules applicable to the audit and certification of educational organization management systems (EOMS) conforming to the requirements given in ISO 21001 (or other sets of specified EOMS requirements). It also provides the necessary information and confidence to customers about the way certification of their suppliers has been granted.
Certification of EOMS is a third-party conformity assessment activity (as described in ISO/IEC 17000:2020, 4.5), and bodies performing this activity are third-party conformity assessment bodies.
NOTE 1 This document can be used as a criteria document for the accreditation or peer assessment of certification bodies which seek to be recognized as being competent to certify that an EOMS conforms to ISO 21001. It is also intended to be used as a criteria document by regulatory authorities and industry consortia which engage in direct recognition of certification bodies to certify that an EOMS conforms to ISO 21001. Some of its requirements could also be useful to other parties involved in the conformity assessment of such certification bodies, and in the conformity assessment of bodies that undertake to certify the compliance of EOMS with criteria additional to, or other than, those in ISO 21001.
NOTE 2 Certification of an EOMS according to ISO 21001 is a management system certification, not a product certification.
NOTE 3 ISO 21001 is a standalone management system standard, not a sector application of ISO 9001.

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1.1   General
This document defines requirements for the preparation and execution of the audit process. In addition, it defines the content and composition for the audit reporting of conformity and process effectiveness to the EN 9100-series standards, the organization’s QMS documentation, and customer and statutory/regulatory requirements.
The requirements in this document are additions or represent changes to the requirements and guidelines in the standards for conformity assessment, auditing, and certification as published by ISO/IEC (i.e. ISO/IEC 17000:2020, ISO/IEC 17021 1). When there is conflict with these standards, the requirements of this document take precedence.
NOTE 1   In this document, the term “EN 9100-series standards” comprises the EN 9100, EN 9110, and EN 9120 standards; developed by the IAQG and published by various national standards bodies.
NOTE 2   In addition to this document, the IAQG publishes deployment support material on the IAQG website (see http://www.iaqg.org) that can be used by audit teams, when executing the audit process.
1.2   Application
This document is intended to be used for audits of EN 9100-series standards by Certification Bodies (CBs) for certification of organizations, under the auspices of the ASD industry certification scheme [also known as the Industry Controlled Other Party (ICOP) scheme]. The ICOP scheme requirements are defined in the EN 9104-series standards (i.e. FprEN 9104-1, prEN 9104-2, EN 9104 3).
NOTE   Relevant parts of this document can also be used by an organization in support of internal audits (1st party) and external audits at suppliers (2nd party).

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This document defines the rules applicable to the audit and certification of educational organization management systems (EOMS) conforming to the requirements given in ISO 21001 (or other sets of specified EOMS requirements). It also provides the necessary information and confidence to customers about the way certification of their suppliers has been granted. Certification of EOMS is a third-party conformity assessment activity (as described in ISO/IEC 17000:2020, 4.5), and bodies performing this activity are third-party conformity assessment bodies. NOTE 1 This document can be used as a criteria document for the accreditation or peer assessment of certification bodies which seek to be recognized as being competent to certify that an EOMS conforms to ISO 21001. It is also intended to be used as a criteria document by regulatory authorities and industry consortia which engage in direct recognition of certification bodies to certify that an EOMS conforms to ISO 21001. Some of its requirements could also be useful to other parties involved in the conformity assessment of such certification bodies, and in the conformity assessment of bodies that undertake to certify the compliance of EOMS with criteria additional to, or other than, those in ISO 21001. NOTE 2 Certification of an EOMS according to ISO 21001 is a management system certification, not a product certification. NOTE 3 ISO 21001 is a standalone management system standard, not a sector application of ISO 9001.

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  • Technical specification
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This document specifies baseline requirements for demonstrating processing activities compliance with the European personal data protection normative framework in accordance with EN ISO/IEC 17065. It does not however apply to products or management systems destined for processing personal data.
This document is applicable to all organizations which, as personal data controllers and/or processors, process personal data, and its objective is to provide a set of requirements enabling such organizations to conform effectively with the European personal data protection normative framework.
An organization can decide that the standard is applicable only to a specific subset of its processing activities if such a decision does not involve failure to conform with the European personal data protection normative framework.
This document also provides indications for conformity assessment with the aforementioned requirements.

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This document gives guidance and requirements for the assessment of conformity of compounds, products, joints and assemblies in accordance with the applicable part(s) of the ISO 16486 series which are intended to be included in the manufacturer’s quality plan as part of the quality management system and for the establishment of certification procedures.
NOTE 1    A basic test matrix in Annex B provides an overview of the testing scheme.
It is recommended for the manufacturer to have a management system such as ISO 9001[4] or equivalent.
NOTE 2    If certification is involved, certification bodies and inspection bodies operating according to ISO/IEC 17065 and ISO/IEC 17020 are considered to be competent.
In conjunction with the other parts of the ISO 16486 series (see Clause 2), this document is applicable to unplasticized polyamide (PA-U) piping systems intended to be buried and used for the supply of gaseous fuels. It is applicable to PA-U pipes, fittings and valves, as well as to their joints and to joints with components of other materials intended to be used under the following conditions:
a)    a maximum operating pressure (MOP) up to and including 18 bar[1] (the MOP is limited to 16 bar for CEN member countries, where ISO 16486-6 is replaced by CEN/TS 12007-6[1]);
b)    an operating temperature of 20 °C as the reference temperature.
NOTE 3    For operating temperatures different to 20 °C, derating coefficients can be used (see ISO 16486-6). CEN member countries use CEN/TS 12007-6[1] and ISO/TS 16486-7 (this document) as a basis, but they can also request additional requirements. For non-CEN member countries, information for dealing with special cases for PA-U can be found in ISO/TS 16486-7 (this document) and PPI TR-3.[7]
For mechanical fittings conforming to ISO 17885, guidance for assessment of conformity is not given in this document. When requested, a quality plan based on the tests mentioned can be set up in agreement between user and manufacturer.
The ISO 16486 series covers a range of maximum operating pressures and gives requirements concerning colours.
NOTE 4    It is the responsibility of the purchaser or specifier to make the appropriate selections from these aspects, taking into account their particular requirements and any relevant national regulations and installation practices or codes.
[1] 1 bar = 0,1 MPa = 105 Pa; 1 MPa = 1 N/mm2.

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This document specifies the general principles of certification, including common procedures and requirements, for the certification of air quality monitoring equipment (AQME).
This document applies to the certification of AQME for ambient air quality and emissions from stationary sources for which performance criteria and test procedures are available in European Standards.
This document provides for the certification of AQME according to the requirements of EN ISO/IEC 17065:2012.
This document elaborates and supplements the requirements of EN ISO/IEC 17065:2012 for bodies certifying AQME. It specifies requirements on testing laboratories as well as the manufacturer’s quality management system (QMS) and the surveillance for the manufacturing process as part of the certification process.

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This document gives guidance and requirements for the assessment of conformity of compounds, products, joints and assemblies in accordance with the applicable part(s) of the ISO 16486 series which are intended to be included in the manufacturer’s quality plan as part of the quality management system and for the establishment of certification procedures.
NOTE 1    A basic test matrix in Annex B provides an overview of the testing scheme.
It is recommended for the manufacturer to have a management system such as ISO 9001[4] or equivalent.
NOTE 2    If certification is involved, certification bodies and inspection bodies operating according to ISO/IEC 17065 and ISO/IEC 17020 are considered to be competent.
In conjunction with the other parts of the ISO 16486 series (see Clause 2), this document is applicable to unplasticized polyamide (PA-U) piping systems intended to be buried and used for the supply of gaseous fuels. It is applicable to PA-U pipes, fittings and valves, as well as to their joints and to joints with components of other materials intended to be used under the following conditions:
a)    a maximum operating pressure (MOP) up to and including 18 bar[1] (the MOP is limited to 16 bar for CEN member countries, where ISO 16486-6 is replaced by CEN/TS 12007-6[1]);
b)    an operating temperature of 20 °C as the reference temperature.
NOTE 3    For operating temperatures different to 20 °C, derating coefficients can be used (see ISO 16486-6). CEN member countries use CEN/TS 12007-6[1] and ISO/TS 16486-7 (this document) as a basis, but they can also request additional requirements. For non-CEN member countries, information for dealing with special cases for PA-U can be found in ISO/TS 16486-7 (this document) and PPI TR-3.[7]
For mechanical fittings conforming to ISO 17885, guidance for assessment of conformity is not given in this document. When requested, a quality plan based on the tests mentioned can be set up in agreement between user and manufacturer.
The ISO 16486 series covers a range of maximum operating pressures and gives requirements concerning colours.
NOTE 4    It is the responsibility of the purchaser or specifier to make the appropriate selections from these aspects, taking into account their particular requirements and any relevant national regulations and installation practices or codes.
[1] 1 bar = 0,1 MPa = 105 Pa; 1 MPa = 1 N/mm2.

  • Technical specification
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This document gives guidance and requirements for the assessment of conformity of compounds, products, joints and assemblies in accordance with the applicable part(s) of the ISO 16486 series which are intended to be included in the manufacturer’s quality plan as part of the quality management system and for the establishment of certification procedures. NOTE 1 A basic test matrix in Annex B provides an overview of the testing scheme. It is recommended for the manufacturer to have a management system such as ISO 9001[4] or equivalent. NOTE 2 If certification is involved, certification bodies and inspection bodies operating according to ISO/IEC 17065 and ISO/IEC 17020 are considered to be competent. In conjunction with the other parts of the ISO 16486 series (see Clause 2), this document is applicable to unplasticized polyamide (PA-U) piping systems intended to be buried and used for the supply of gaseous fuels. It is applicable to PA-U pipes, fittings and valves, as well as to their joints and to joints with components of other materials intended to be used under the following conditions: a) a maximum operating pressure (MOP) up to and including 18 bar[1] (the MOP is limited to 16 bar for CEN member countries, where ISO 16486-6 is replaced by CEN/TS 12007-6[1]); b) an operating temperature of 20 °C as the reference temperature. NOTE 3 For operating temperatures different to 20 °C, derating coefficients can be used (see ISO 16486-6). CEN member countries use CEN/TS 12007-6[1] and ISO/TS 16486-7 (this document) as a basis, but they can also request additional requirements. For non-CEN member countries, information for dealing with special cases for PA-U can be found in ISO/TS 16486-7 (this document) and PPI TR-3.[7] For mechanical fittings conforming to ISO 17885, guidance for assessment of conformity is not given in this document. When requested, a quality plan based on the tests mentioned can be set up in agreement between user and manufacturer. The ISO 16486 series covers a range of maximum operating pressures and gives requirements concerning colours. NOTE 4 It is the responsibility of the purchaser or specifier to make the appropriate selections from these aspects, taking into account their particular requirements and any relevant national regulations and installation practices or codes. [1] 1 bar = 0,1 MPa = 105 Pa; 1 MPa = 1 N/mm2.

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This document specifies general requirements for the competence and impartiality of proficiency
testing (PT) providers and consistent operation of all proficiency testing schemes. This document can
be used as a basis for specific technical requirements for particular fields of application.
Users of proficiency testing schemes, regulatory authorities, organizations and schemes using peer-
assessment, accreditation bodies and others can use these requirements in confirming or recognizing
the competence of proficiency testing providers.

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  • Standard
    47 pages
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This document specifies general requirements for the competence and impartiality of proficiency
testing (PT) providers and consistent operation of all proficiency testing schemes. This document can
be used as a basis for specific technical requirements for particular fields of application.
Users of proficiency testing schemes, regulatory authorities, organizations and schemes using peer-
assessment, accreditation bodies and others can use these requirements in confirming or recognizing
the competence of proficiency testing providers.

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  • Standard
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This document specifies general requirements for the competence and impartiality of proficiency testing (PT) providers and consistent operation of all proficiency testing schemes. This document can be used as a basis for specific technical requirements for particular fields of application. Users of proficiency testing schemes, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies and others can use these requirements in confirming or recognizing the competence of proficiency testing providers.

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This document, the audit data collection standard (ADCS), defines the functional requirements for exchanging audit data in flat file format. This document concerns the specification of technical exchange formats in extensible markup language (XML), JavaScript object notation (JSON) and comma-separated values (CSV) as output file formats for the functional content defined in ISO 21378. This document also contains the following schemas and sample files for tables in ISO 21378. — XML schema; — XML sample file; — JSON schema; — JSON sample file. To keep the three exchange formats (XML, JSON and CSV) consistent, this document also specifies how to use the technical solution in the CSV format.

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This document specifies requirements for the management of farmed Angora rabbits in accordance with animal welfare principles.
This document applies to the management and control of critical activities in Angora rabbit farming, including accommodation, reproduction, feed and nutrients, health, fibre collection, ethical claims and supporting information.

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This document specifies requirements for the management of farmed Angora rabbits in accordance with animal welfare principles.
This document applies to the management and control of critical activities in Angora rabbit farming, including accommodation, reproduction, feed and nutrients, health, fibre collection, ethical claims and supporting information.

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This document specifies requirements for the management of farmed Angora rabbits in accordance with animal welfare principles. This document applies to the management and control of critical activities in Angora rabbit farming, including accommodation, reproduction, feed and nutrients, health, fibre collection, ethical claims and supporting information.

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This document provides a framework that organisations can follow, and that can be used as the structure for market or sector specific schemes. It is intended to be a process certification.
The goal of this document is to have comparable attestations or certifications worldwide.

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