| Code of Conduct (CoC) | Code of Conduct for Notified Bodies under Directives 90/385/EEC, 93/42/EEC,98/79/EC, EU 2017/745 and EU 2017/746 | TR | 4.0 | 2019-10-01 | -- |
| EA-2/17 | EA Guidance on the horizontal requirements for the accreditation of conformity assessment bodies for notification purposes | | rev. 04 | 2020-04-17 | Informative (former version was mandatory). |
| EA-4/02 | Expression of the uncertainty of measurement in calibration | | rev. 03 | 2022-04-04 | Mandatory |
 EA-4/16 | EA guidelines on the expression of uncertainty in quantitative testing | | rev. 00 | 2003-12-01 | Guidance |
| FCC Technical Assessment Checklist (Publication nr: 853844) | This checklist is intended to serve as a guide and provide a minimum list of items to be included in the technical evaluation of the test laboratory, as part of the complete ISO/IEC 17025 assessment for an accredited testing laboratory. | | v02r01 | 2018-03-02 | -- |
| IAF GD5 | IAF Guidance on the Application of ISO/IEC Guide 65:1996 | | 3 | 2006-12-01 | Withdrawn |
| IAF MD 1 | Audit and Certification of a Management System Operated by a Multi-Site Organization | | issue 3 | 2023-10-18 | -- |
| IAF MD 10 | IAF Mandatory Document for Assessment of Certification Body Management of Competence in Accordance with ISO/IEC 17021:2011 | | NA- | 2013-02-11 | Withdrawn |
| IAF MD 11 | IAF Mandatory Document for the Application of ISO/IEC 17021 for Audits of Integrated Management Systems (IMS) | | issue 1, v4 | 2023-06-16 | -- |
| IAF MD 12 | Accreditation Assessment of Conformity Assessment Bodies with Activities in Multiple Countries | | issue 2, v2 | 2023-06-14 | -- |
| IAF MD 15 | IAF Mandatory Document for the Collection of Data to Provide Indicators of Management System Certification Bodies' Performance | | issue 1, v2 | 2023-06-14 | -- |
| IAF MD 2 | IAF Mandatory Document for the Transfer of Accredited Certification of Management Systems | | issue 2, v2 | 2023-06-14 | -- |
| IAF MD 4 | Use of Information and Communication Technology (ICT) for Auditing/Assessment Purposes | | issue 2, v4 | 2022-02-01 | -- |
| IAF MD 5 | Determination of Audit Time of Quality and Environmental Management Systems | | issue 4, v3 | 2023-06-14 | -- |
| IAF MD 7 | Harmonization of Sanctions and Dealing with Fraudulent Behaviour | | issue 2, v2 | 2023-07-19 | -- |
| IAF MD 9 | Application of ISO/IEC/IEC 17021-1 in the Field of Medical Device Quality Management Systems (ISO/IEC 13485) | | issue 4, version 2 | 2023-06-14 | -- |
| ILAC G13 | Guidelines for the Requirements for the Competence of Providers of Proficiency Testing Schemes | | NA- | 2007-08-01 | Withdrawn |
| ISO Guide 67 | Conformity assessment - Fundamentals of product certification | | NA- | 2004-09-01 | Withdrawn (revised by ISO/IEC 17067:2013) |
| ISO/IEC 17007 | Conformity assessment - Guidance for drafting normative documents suitable for use for conformity assessment | | 1 | 2009-10-01 | Supersedes ISO/IEC Guide 7:1994 |
| ISO/IEC 17021-1 | Conformity assessment - Requirements for bodies providing audit and certification of management systems - Part 1: Requirements | | NA- | 2015-07-01 | -- |
| ISO/IEC 17021-3 | Conformity assessment - Requirements for bodies providing audit and certification of management systems - Part 3: Competence requirements for auditing and certification of quality management systems | | NA- | 2018-12-01 | -- |
| ISO/IEC 17025 | General requirements for the competence of testing and calibration laboratories | | NA- | 2018-01-01 | Supersedes NEN-EN-ISO/IEC 17025:2005 |
| ISO/IEC 17025 /C1 (Usage in combination with ISO/IEC 17025:2 | General requirements for the competence of testing and calibration laboratories | C | NA- | 2007-01-01 | Usage in combination with ISO/IEC 17025:2005. Supersedes ISO/IEC 17025:2005 /C1:2006 |
| ISO/IEC 17065 | Conformity assessment - Requirements for bodies certifying products, processes and services | | NA- | 2012-09-01 | Replaces NEN-EN 45011:1998 and ISO/IEC Guide 65:1996 |
| ISO/IEC 17067 | Conformity assessment -- Fundamentals of product certification and guidelines for product certification schemes | | 1 | 2013-08-01 | Replaces ISO Guide 67 |
| ISO/IEC TS 17023 | Conformity assessment -- Guidelines for determining the duration of management system certification audits | B | NA- | 2013-08-01 | -- |
| JCGM 100:2008 | Evaluation of measurement data - Guide to the expression of uncertainty in measurement | | NA- | 2008-09-01 | GUM 1995 with minor corrections |
| LAB34 | The Expression of Uncertainly in EMC Testing | | 1 | 2012-11-01 | -- |
| NEN-EN 45011 | General requirements for bodies operating product certification systems | | NA- | 1998-03-01 | Withdrawn (replaced by ISO/IEC 17065:2012) |
| NEN-EN 45020 | Standardization and related activities - General vocabulary | | NA- | 2007-01-01 | Replaces ISO Guide 2:2005 |
| NEN-EN-ISO/IEC 10012 | Measurement management systems - Requirements for the measurement processes and measuring equipment | | NA- | 2003-05-01 | Supersedes EN 10012- 2:1997 |
| NEN-EN-ISO/IEC 19011 | Guidelines for auditing management systems | G | NA- | 2018-07-01 | Supersedes NEN-EN-ISO/IEC 19011:2002 |
| NEN-ISO/IEC 10006 | Quality management systems - Guidelines for quality management in projects | | NA- | 2017-11-01 | Supersedes NEN-ISO/IEC 10006:2003 |
| SAP-C000 | Accreditatie van Certificatie van Managementsystemen | | NA- | 2019-10-28 | Replaces version 4, 13-11-2018 |
| SAP-C021 | Certificatie volgens ISO/IEC 13485 (medische hulpmiddelen) (Engelstalig) | | NA- | 2021-07-06 | -- |
| T040 | Toelichting op uitvoering van RvA-beoordelingsinstrument ‘schaduwonderzoeken’ | | NA- | 2020-01-07 | -- |
| T051 | Management of extraordinary events or circumstances affecting RvA accredited bodies and their customers | A | 6.0 | 2020-11-03 | -- |
| VR003 | Voorschrift voor het gebruik van Accreditatiemerken en logo's | | 6.0 | 2020-12-15 | -- |
