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.

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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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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 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 and provides guidance for bodies providing audit and certification of a privacy information management system (PIMS) according to ISO/IEC 27701 in combination with ISO/IEC 27001, in addition to the requirements contained within ISO/IEC 27006 and ISO/IEC 27701. It is primarily intended to support the accreditation of certification bodies providing PIMS certification.
The requirements contained in this document need to be demonstrated in terms of competence and reliability by anybody providing PIMS certification, and the guidance contained in this document provides additional interpretation of these requirements for any body 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 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 and provides guidance for bodies providing audit and certification of a privacy information management system (PIMS) according to ISO/IEC 27701 in combination with ISO/IEC 27001, in addition to the requirements contained within ISO/IEC 27006 and ISO/IEC 27701. It is primarily intended to support the accreditation of certification bodies providing PIMS certification.
The requirements contained in this document need to be demonstrated in terms of competence and reliability by anybody providing PIMS certification, and the guidance contained in this document provides additional interpretation of these requirements for any body 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 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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ISO/IEC 27007 provides guidance on managing an information security management system (ISMS) audit programme, on conducting audits, and on the competence of ISMS auditors, in addition to the guidance contained in ISO 19011:2011.
ISO/IEC 27007 is applicable to those needing to understand or conduct internal or external audits of an ISMS or to manage an ISMS audit programme.

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This document specifies the requirements for the audit and certification of a food safety management system (FSMS) complying with the requirements given in ISO 22000 (or other specified FSMS requirements). It also provides the necessary information and confidence to customers about the way certification of their suppliers has been granted. Certification of FSMS is a third-party conformity assessment activity (as described in ISO/IEC 17000:2020, 4.3), and bodies performing this activity are third-party conformity assessment bodies. NOTE 1 In this document, the terms “product” and “service” are used separately (in contrast with the definition of “product” given in ISO/IEC 17000). NOTE 2 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 FSMS complies with ISO 22000 or other sets of specified FSMS requirements. 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 FSMS complies with ISO 22000. Some of its requirements can 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 FSMS with criteria additional to, or other than, those in ISO 22000. FSMS certification does not attest to the safety or fitness of the products of an organization within the food chain. However, an FSMS requires an organization to meet all applicable food-safety-related statutory and regulatory requirements through its management system. NOTE 3 Certification of an FSMS according to ISO 22000 is a management system certification, not a product certification. Other FSMS users can use the concepts and requirements of this document provided that the requirements are adapted as necessary.

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This document is supplemental to ISO/IEC 17065. It specifies the rules applicable for the audit of a food safety system (FSS) and certification of products, processes and services complying with requirements of a certification scheme that is based on the internationally accepted principles of food safety (e.g. CODEX General Principles of Food Hygiene[8]) and includes management system elements. This document does not apply to certifications that are solely based on product testing (e.g. performed by an organization applying ISO/IEC 17025) or inspection (e.g. performed by an organization applying ISO/IEC 17020) and does not apply to ISO/IEC 17065-based food safety schemes that do not include both internationally accepted principles of food safety and management system elements. It also provides the necessary information and confidence to customers about the way certification of their suppliers has been granted. Certification of FSS is a third-party conformity assessment activity (as described in ISO/IEC 17000:2020, 4.3) and bodies performing this activity are third-party conformity assessment bodies. NOTE 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 organization’s products, processes and services and its FSS comply with the requirements of a certification scheme. 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 organization’s FSS complies with a certification scheme’s requirements. Some of its requirements can 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 an FSS with additional criteria. FSS certification does not attest to the safety or fitness of the products of an organization within the food chain. However, certification requires an organization to meet all applicable food-safety-related statutory and regulatory requirements through its FSS.

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This document recommends good practices for all elements of conformity assessment, including objects of conformity assessment, specified requirements, activities, bodies, systems, schemes and results. It is intended for use by individuals and bodies that wish to provide, promote or use impartial and reliable conformity assessment services. Providers of conformity assessment can include conformity assessment bodies, accreditation bodies, peer-assessment agreement groups, and organizations providing declarations of conformity. Individuals or organizations that promote or use conformity assessment can include, as appropriate, regulators, trade officials, and owners of conformity assessment systems and schemes.

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In addition to the guidelines in ISO 19011, this document provides guidelines to organizations that contribute to the achievement of road vehicle cybersecurity throughout the supply chain on: — managing an audit programme for a cybersecurity management system (CSMS); — conducting organizational CSMS audits; — competencies of CSMS auditors; and — providing evidence during CSMS audits. Elements of the CSMS are based on the processes described in ISO/SAE 21434. This document is applicable to those needing to understand or conduct internal or external audits of a CSMS or to manage a CSMS audit programme. This document does not provide guidelines on cybersecurity assessments.

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This document provides general requirements for third-party marks of conformity, including their
issue and use.
This document is applicable to third-party marks of conformity issued and used in different forms and
various media, including digital representation employing electronically stored and displayed marks,
machine readable code, blockchain (distributed ledger) or other electronic means.
NOTE 1 This document can also be used as guidance in using marks of conformity in activities other than
third-party conformity assessment.
NOTE 2 Third-party marks of conformity in accordance with this document also include symbols of
recognition, such as accreditation symbols. For consistency of terminology, they are referred to as accreditation
marks.
NOTE 3 Third-party marks of conformity in accordance with this document can include logos (e.g. the sign of
a conformity assessment body or trademarks), symbols (e.g. the representation of recognition in an accreditation
agreement or the depiction of the applicable programme) or a combination thereof.
NOTE 4 Third-party marks of conformity as a graphic representation of demonstrated conformity in
accordance with this document can be a combination of multiple marks (e.g. indications of compliance with
several sets of specifications, codes for individually fulfilled specifications).
NOTE 5 This document does not apply to markings that provide indication of a designation, a code, or a
classification only. Furthermore, it does not apply to graphic representations (e.g. of conformity assessment
systems or schemes/programmes) or logos (e.g. of an association of accreditation bodies or an association of
conformity assessment bodies).
NOTE 6 Third-party marks of conformity are based on a conformity assessment scheme that includes the
function of surveillance.

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ISO/IEC 27007 provides guidance on managing an information security management system (ISMS) audit programme, on conducting audits, and on the competence of ISMS auditors, in addition to the guidance contained in ISO 19011:2011.
ISO/IEC 27007 is applicable to those needing to understand or conduct internal or external audits of an ISMS or to manage an ISMS audit programme.

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This document specifies the requirements for competence to carry out reference measurement procedures in laboratory medicine, using the requirements of ISO/IEC 17025:2017 as a normative reference and listing additional requirements for calibration laboratories to perform their tasks adequately.
The relationship between clauses in this document and ISO/IEC 17025:2017 are summarized in Annex A.
Examinations of properties with results reported on a nominal or ordinal scale are not included.
This document is not applicable to medical laboratories.
NOTE       Requirements for medical laboratories are specified in ISO 15189[1].

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This document specifies the International Standards, including clauses and subclauses, with which
conformity to the quality requirements of ISO 3834-2, ISO 3834-3 or ISO 3834-4 can be claimed.
NOTE For brazing, see ISO 22688.

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This document specifies the competence requirements for personnel involved in the audit and certification process for management systems for records (MSR). It complements the existing requirements of ISO/IEC 17021-1. NOTE This document is applicable for auditing and certification of MSR based on ISO 30301. It can also be used for other MSR applications.

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This document specifies principles and requirements for bodies performing validation and verification
of environmental information statements.
Any programme requirements related to bodies are additional to the requirements of this document.
This document is a sector application of ISO/IEC 17029:2019, which contains general principles
and requirements for the competence, consistent operation and impartiality of bodies performing
validation/verification as conformity assessment activities.
This document includes sector-specific requirements in addition to the requirements of
ISO/IEC 17029:2019.

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This document specifies the competence requirements for personnel involved in the audit and certification process for compliance management systems (CMS). It complements the existing requirements of ISO/IEC 17021‑1.

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This document provides general requirements for third-party marks of conformity, including their
issue and use.
This document is applicable to third-party marks of conformity issued and used in different forms and
various media, including digital representation employing electronically stored and displayed marks,
machine readable code, blockchain (distributed ledger) or other electronic means.
NOTE 1 This document can also be used as guidance in using marks of conformity in activities other than
third-party conformity assessment.
NOTE 2 Third-party marks of conformity in accordance with this document also include symbols of
recognition, such as accreditation symbols. For consistency of terminology, they are referred to as accreditation
marks.
NOTE 3 Third-party marks of conformity in accordance with this document can include logos (e.g. the sign of
a conformity assessment body or trademarks), symbols (e.g. the representation of recognition in an accreditation
agreement or the depiction of the applicable programme) or a combination thereof.
NOTE 4 Third-party marks of conformity as a graphic representation of demonstrated conformity in
accordance with this document can be a combination of multiple marks (e.g. indications of compliance with
several sets of specifications, codes for individually fulfilled specifications).
NOTE 5 This document does not apply to markings that provide indication of a designation, a code, or a
classification only. Furthermore, it does not apply to graphic representations (e.g. of conformity assessment
systems or schemes/programmes) or logos (e.g. of an association of accreditation bodies or an association of
conformity assessment bodies).
NOTE 6 Third-party marks of conformity are based on a conformity assessment scheme that includes the
function of surveillance.

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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 is recommended for use 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 is recommended for use as a criteria document for accreditation, peer assessment or other audit processes.

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This document provides general requirements for third-party marks of conformity, including their issue and use. This document is applicable to third-party marks of conformity issued and used in different forms and various media, including digital representation employing electronically stored and displayed marks, machine readable code, blockchain (distributed ledger) or other electronic means. NOTE 1 This document can also be used as guidance in using marks of conformity in activities other than third-party conformity assessment. NOTE 2 Third-party marks of conformity in accordance with this document also include symbols of recognition, such as accreditation symbols. For consistency of terminology, they are referred to as accreditation marks. NOTE 3 Third-party marks of conformity in accordance with this document can include logos (e.g. the sign of a conformity assessment body or trademarks), symbols (e.g. the representation of recognition in an accreditation agreement or the depiction of the applicable programme) or a combination thereof. NOTE 4 Third-party marks of conformity as a graphic representation of demonstrated conformity in accordance with this document can be a combination of multiple marks (e.g. indications of compliance with several sets of specifications, codes for individually fulfilled specifications). NOTE 5 This document does not apply to markings that provide indication of a designation, a code, or a classification only. Furthermore, it does not apply to graphic representations (e.g. of conformity assessment systems or schemes/programmes) or logos (e.g. of an association of accreditation bodies or an association of conformity assessment bodies). NOTE 6 Third-party marks of conformity are based on a conformity assessment scheme that includes the function of surveillance.

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This document provides criteria to assess conformity of the built environment with the functional requirements and recommendations described in EN 17210 Accessibility and usability of the built environment – Functional requirements, regardless of whether self-declaration, second-party attestation or third-party certification is requested.
This document provides guidance on how and when accessibility and usability of the built environment have to be considered throughout all stages of the building process, including feasibility, design, construction, completion and post occupancy. It is also applicable for refurbishment or adaptation of existing buildings.
FprCEN/TR 17621 Accessibility and usability of the built environment - Technical performance criteria and specifications, provides examples of a way or ways in which the functional requirements in EN 17210 could be fulfilled. Alternatively, National Standards or Regulations can determine the technical performance criteria and specifications to fulfil the functional requirements of/in EN 17210.
NOTE 1    Design for All, Inclusive Design and Universal Design share a similar inclusive design philosophy. “Universal Design” means the design of products, environments, programmes and services to be usable by all people, to the greatest extent possible, without the need for adaptation or specialized design. “Universal Design” does not exclude assistive options or devices for particular groups of persons with disabilities where this is needed.
NOTE 2    Terms such as "design for all", “inclusive Design”, "universal design", "accessible design", "barrier-free design", "inclusive design" and "transgenerational design" are often used interchangeably with the same meaning.

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This document specifies requirements and provides guidance for certification bodies providing audit and certification of an ITAMS in accordance with ISO/IEC 19770-1. It does not change the requirements specified in ISO/IEC 19770-1. This document can also be used by accreditation bodies for the accreditation of certification bodies. However, this document does not specify requirements or provides guidance for accreditation bodies to audit certification bodies. A certification body providing ITAMS certification is expected to be able to demonstrate fulfilment of the requirements specified in this document, in addition to the requirements in ISO/IEC 17021-1.

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This International Standard 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 and ISO/IEC 27001. It is primarily intended to support
the accreditation of certification bodies providing ISMS certification.
The requirements contained in this International Standard need to be demonstrated in terms of
competence and reliability by any body providing ISMS certification, and the guidance contained in
this International Standard provides additional interpretation of these requirements for any body
providing ISMS certification.
NOTE This International Standard can be used as a criteria document for accreditation, peer assessment or
other audit processes.

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This document specifies requirements for competence, consistency and impartiality in the auditing and certification of ISO 50001 energy management systems (EnMS) for bodies providing these services. In order to ensure the effectiveness of EnMS auditing, this document addresses the auditing process, the competence requirements for the personnel involved in the certification process for EnMS, the audit time and multi-site sampling.

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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 combination with ISO/IEC 27001, in addition to the requirements contained within ISO/IEC 27006 and ISO/IEC 27701. It is primarily intended to support the accreditation of certification bodies providing PIMS certification. The requirements contained in this document need to be demonstrated in terms of competence and reliability by anybody providing PIMS certification, and the guidance contained in this document provides additional interpretation of these requirements for any body 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 International Standard 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 and ISO/IEC 27001. It is primarily intended to support
the accreditation of certification bodies providing ISMS certification.
The requirements contained in this International Standard need to be demonstrated in terms of
competence and reliability by any body providing ISMS certification, and the guidance contained in
this International Standard provides additional interpretation of these requirements for any body
providing ISMS certification.
NOTE This International Standard can be used as a criteria document for accreditation, peer assessment or
other audit processes.

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This document specifies general terms and definitions relating to conformity assessment (including the
accreditation of conformity assessment bodies) and to the use of conformity assessment to facilitate trade.
The general principles of conformity assessment and a description of the functional approach to
conformity assessment are provided in Annex A.
Conformity assessment interacts with other fields such as management systems, metrology,
standardization and statistics. The boundaries of conformity assessment are not defined in this
document.

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ISO/IEC 17011:2017 specifies requirements for the competence, consistent operation and impartiality of accreditation bodies assessing and accrediting conformity assessment bodies.

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ISO/IEC 17025:2017 specifies the general requirements for the competence, impartiality and consistent operation of laboratories.
ISO/IEC 17025:2017 is applicable to all organizations performing laboratory activities, regardless of the number of personnel.
Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use ISO/IEC 17025:2017 in confirming or recognizing the competence of laboratories.

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This European Standard establishes a semantic data model of the core elements of an electronic invoice. The semantic model includes only the essential information elements that an electronic invoice needs to ensure legal (including fiscal) compliance and to enable interoperability for cross-border, cross sector and for domestic trade. The semantic model may be used by organizations in the private and the public sector for public procurement invoicing. It may also be used for invoicing between private sector enterprises. It has not been specifically designed for invoicing consumers.
This European Standard complies at least with the following criteria:
-   it is technologically neutral;
-   it is compatible with relevant international standards on electronic invoicing;
-   the application of this standard should comply with the requirements for the protection of personal data of Directive 95/46/EC, having due regard to the principles of privacy and data protection by-design, data minimization, purpose limitation, necessity and proportionality;
-   it is consistent with the relevant provisions of Directive 2006/112/EC [2];
-   it allows for the establishment of practical, user-friendly, flexible and cost-efficient electronic invoicing systems;
-   it takes into account the special needs of small and medium-sized enterprises as well as of sub-central contracting authorities and contracting entities;
-   it is suitable for use in commercial transactions between enterprises.

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This document specifies general terms and definitions relating to conformity assessment (including the
accreditation of conformity assessment bodies) and to the use of conformity assessment to facilitate trade.
The general principles of conformity assessment and a description of the functional approach to
conformity assessment are provided in Annex A.
Conformity assessment interacts with other fields such as management systems, metrology,
standardization and statistics. The boundaries of conformity assessment are not defined in this
document.

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  • Standard – translation
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This document contains general principles and requirements for the competence, consistent operation and impartiality of bodies
providing validation and verification as conformity assessment.
Bodies operating to this document can be internal (first party), collaborative (second party) as well as independent (third party) bodies
and need not offer both, validation and verification activities.
This document is applicable to validation and verification bodies in any sector, providing assurance through confirmation that claims or
declarations are either plausible with regard to the intended purpose (validation) or correctly stated (verification).
This document shall be applied in conjunction with sector specific programmes that contain requirements for validation and verification
processes and rules.
This document can be used as a basis for accreditation by accreditation bodies, peer assessment within peer assessment groups, or
other forms of recognition of validation and verification bodies by international or regional organizations, governments, regulatory
authorities, program or scheme owners, industry bodies, companies, customers or consumers.
NOTE This document contains generic requirements and is neutral with regard to the operated validation or verification programme. Requirements of
the applicable programmes are additional to the requirements of this document.

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    70 pages
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    33 pages
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This document specifies general terms and definitions relating to conformity assessment (including the accreditation of conformity assessment bodies) and to the use of conformity assessment to facilitate trade. The general principles of conformity assessment and a description of the functional approach to conformity assessment are provided in Annex A. Conformity assessment interacts with other fields such as management systems, metrology, standardization and statistics. The boundaries of conformity assessment are not defined in this document.

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2020-03-23: corrigendum created to confirm EN 61400-22:2011 and is not the result of a mistake (see BT decision D165/C016)

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This document specifies additional competence requirements for personnel involved in the audit and certification process of collaborative business relationship management systems (CBRMS) and complements the existing requirements of ISO/IEC 17021-1.

  • Technical specification
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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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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 is recommended for use as a criteria document for accreditation, peer assessment or other audit processes.

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This document provides guidance on managing an information security management system (ISMS) audit programme, on conducting audits, and on the competence of ISMS auditors, in addition to the guidance contained in ISO 19011. This document is applicable to those needing to understand or conduct internal or external audits of an ISMS or to manage an ISMS audit programme.

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This document specifies requirements for certification schemes for sustainable and traceable cocoa, including the certification of cocoa bean producing organizations and cocoa supply chain actors. It is to be used jointly with ISO 34101-1, ISO 34101-2 and/or ISO 34101-3.
This document also specifies the requirements for cocoa sustainability management systems:
—          at entry level, see Annex A;
—          at medium level, see Annex B.
NOTE       ISO 34101-1 specifies the requirements for cocoa sustainability management systems at high level.
Only organizations that fulfil both the cocoa sustainability management system requirements of either ISO 34101-1 or Annex A or B, and the performance requirements of ISO 34101-2 can claim their cocoa beans have been sustainably produced.

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This document contains general principles and requirements for the competence, consistent operation and impartiality of bodies
providing validation and verification as conformity assessment.
Bodies operating to this document can be internal (first party), collaborative (second party) as well as independent (third party) bodies
and need not offer both, validation and verification activities.
This document is applicable to validation and verification bodies in any sector, providing assurance through confirmation that claims or
declarations are either plausible with regard to the intended purpose (validation) or correctly stated (verification).
This document shall be applied in conjunction with sector specific programmes that contain requirements for validation and verification
processes and rules.
This document can be used as a basis for accreditation by accreditation bodies, peer assessment within peer assessment groups, or
other forms of recognition of validation and verification bodies by international or regional organizations, governments, regulatory
authorities, program or scheme owners, industry bodies, companies, customers or consumers.
NOTE This document contains generic requirements and is neutral with regard to the operated validation or verification programme. Requirements of
the applicable programmes are additional to the requirements of this document.

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