European co-operation for Accreditation2023-11-10T11:24:25+01:00

Benefits of the EA MLA

Ongoing development

European accreditation infrastructure

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DIRECTORY

EUROPEAN COMMISSION

DIRECTORY

EUROPEAN COMMISSION

Status Date Reference Description
revised 2024-03-15 EA-INF/01 List of EA Publications and International Documents READ MORE
revised 2024-02-19 EA-1/15 A EA policy for relations with stakeholders READ MORE
revised 2024-03-15 EA-INF/02 Contact Persons of EA Members, Recognized Stakeholders and Observers READ MORE
revised 2024-01-22 EA-INF/03 Signatories to the EA Multilateral Agreement READ MORE
revised 2024-01-18 EA-INF/05 Directory of European legislations and EU schemes with provisions to accreditation and/or conformity assessment READ MORE
revised 2023-11-28 EA-INF/17 Register of EA resolutions for use by EA, National Accreditation Bodies and EA evaluators READ MORE
revised 2023-11-20 EA-2/15 M EA requirements for the accreditation of flexible scopes READ MORE
normal 2023-11-08 EA-1/17 A EA Rules of Procedure READ MORE
new 2023-11-08 EA Code of Conduct READ MORE
normal 2023-07-11 EA-INF/15 Joint EA - EDQM Communication regarding Cooperation when carrying out (joint) audits/assessments in Official Medicines Control Laboratories READ MORE
normal 2023-05-24 EA-1/22 A EA Procedure and Criteria for the Evaluation of Conformity Assessment Schemes by EA Accreditation Body Members READ MORE
normal 2023-05-15 EA-0/07 EA Procedure for application for EA membership and application form READ MORE
normal 2022-12-01 EA-2/02 S3 M Risk-based approach for the planning of a peer evalution READ MORE
normal 2022-12-01 EA-1/13 A EA's relationship with accreditation bodies of countries not being members of the EU or EFTA READ MORE
normal 2022-10-18 EA-2/21 G Guidance on remote assessments READ MORE
normal 2022-09-27 EA-INF/11 Scope of the EA MLA and the application of an EA MLA signatory to join the IAF MLA for a specific mainscope/sub-scope and/or the ILAC MRA for a specific activity READ MORE
normal 2022-07-08 Accredited laboratories for face mask testing READ MORE
normal 2022-06-17 CPR System 3 - Acceptance of test resuts provided by a laboratory accredited in the United Kingdom (UK), being also an Approved Body from UK (17th June 2022) READ MORE
normal 2022-06-14 EA-6/03 M EA document for accreditation of Verification Bodies for the purpose of EU ETS Directive READ MORE
normal 2022-06-10 EA 4/09 G Accreditation For Sensory Testing Laboratories READ MORE
normal 2022-06-10 EA-3/02 M EA policy for the accreditation of Certification Bodies providing certification of PDO, PGI and TSG READ MORE
normal 2022-05-13 EA 2/02 S5 Multilateral Agreement Council Procedure for making the EA MLA decisions by online ballot, in between meetings READ MORE
normal 2022-05-04 EA-2/19 List of risks for accreditation processes and operation of national accreditation bodies READ MORE
normal 2022-04-22 EA-1/17 S5 A-AB Levying of membership fees READ MORE
normal 2022-04-19 EA-2/02 EA Procedure for the evaluation of a National Accreditation Body READ MORE
normal 2022-04-19 EA-1/14 A Procedure for development and approval of EA documents and the adoption of ILAC/IAF documents READ MORE
normal 2022-04-19 EA-1/17 S1 A - AB Criteria for membership READ MORE
normal 2022-04-19 EA-1/17 S3 A Procedure for the investigation and resolution of Complaints and Appeals READ MORE
normal 2022-04-19 EA-1/17 S4 A + AB Proxy procedure READ MORE
normal 2022-04-19 EA-1/19 A - AB Rules for use of EA logo and Graphic Specification READ MORE
normal 2022-04-11 EA-1/06 A-AB EA multilateral agreement - Criteria for signing - Policy and procedures for development READ MORE
normal 2022-04-04 EA-4/02 M Evaluation of the Uncertainty of Measurement in Calibration READ MORE
normal 2022-03-09 EA-3/12 M EA Policy for the Accreditation of Organic Production Certification READ MORE
normal 2022-02-17 EA-4/17 M Description of scopes of accreditation for medical laboratories READ MORE
normal 2022-02-17 EA-2/02 S4 G Procedure for remote peer evaluations during the COVID-19 pandemic READ MORE
normal 2022-02-17 EA 2/02 S1 M Description of competence criteria of the EA Secretariat personnel involved in the management of the peer evaluation process READ MORE
normal 2022-02-17 EA-2/02 S2 M Circumstances and process of involving EA Technical Committees in peer evaluation issues READ MORE
normal 2022-01-10 EA-6/02 M EA Guidelines on the use of ISO/IEC 17065 and ISO/IEC 17021-1 for Certification to EN ISO 3834 READ MORE
normal 2022-01-03 EA-1/20 S1 A-AB Terms and Conditions for Financial Compensation from the Operating Grant to an EA National Accreditation Body READ MORE
normal 2022-01-03 EA-1/20 A EA Procedure for the control of expenditures and preparation of budgets READ MORE
normal 2021-12-08 READ MORE
normal 2021-11-25 Articles of Association READ MORE
normal 2021-11-15 EA-4/18 G Guidance on the level and frequency of proficiency testing participation READ MORE
normal 2021-07-08 EA-0/02 Procedure for Document Control READ MORE
normal 2021-06-02 EA-3/01 M EA Conditions for the use of Accreditation Symbols, Logos and other claims of accreditation and reference to the EA MLA Signatory status READ MORE
normal 2021-05-28 EA-4/20 G Guidance for the assessment of laboratories against EN ISO 15189 and EN ISO 22870 Point-of Care Testing (POCT) READ MORE
normal 2021-05-05 EA-0/10 Procedure for EA meetings READ MORE
normal 2021-04-08 EA-5/02 Guidance on the application of ISO/IEC 17020 in vehicle inspection READ MORE
normal 2021-03-31 EA-INF/09 Guide on the publication of data on accredited verifiers according to article 76 of Commission implementing regulation (EU) No 2018/2067 READ MORE
normal 2021-03-31 EA-INF/10 Guide on the content of the accreditation certificate for verifiers accredited for EN ISO 14065 and the Commission implementing regulation (EU) No 2018/2067 READ MORE
normal 2020-09-21 EA-INF/04 Statement on acceptance and recognition of activities under the EA MLA READ MORE
normal 2020-06-29 EA-INF/07 National Accreditation Body Communication with National Regulators - Best Practice Guide READ MORE
normal 2020-04-17 EA-2/17 M EA Document on Accreditation for Notification purposes READ MORE
normal 2020-04-17 EA-2/20 G Consultancy, and the Independence of Conformity Assessment Bodies READ MORE
normal 2020-03-23 READ MORE
normal 2019-10-16 EA-4/23 INF The Assessment and Accreditation of Opinions and Interpretations using ISO/IEC 17025:2017 READ MORE
normal 2019-07-07 EA-0/09 Procedure for internal audit READ MORE
normal 2019-07-04 EA-4/21 INF Guidelines for the assessment of the appropriateness of small interlaboratory comparisons within the process of laboratory accreditation READ MORE
normal 2019-05-06 EA-2/13 M EA Cross Border Accreditation Policy and Procedure for Cross Border Cooperation between EA Members. READ MORE
normal 2019-03-15 EA-1/23 A EA policy to speak with “One Voice” READ MORE
normal 2018-11-30 EA-4/22 G EA Guidance on Accreditation of Pesticide Residues Analysis in Food and Feed READ MORE
normal 2018-08-09 EA-INF/16 List of most common acronyms and abbreviations used in EA READ MORE
normal 2017-07-11 EA-0/08 Procedure for management reviews READ MORE
normal 2017-05-14 EA-7/04 M Legal Compliance as a part of accredited ISO 14001:2015 certification READ MORE
normal 2015-10-01 EA-INF/14 Communication with EC and its DGs READ MORE
normal 2015-05-26 EA-0/12 Guidelines for implementation of EA Projects READ MORE
normal 2009-04-13 EA-0/06 Format and layout of EA documents READ MORE
normal 2008-07-12 EA-1/21 A-AB EA Internal procedure for liaison activities (previously EA-0/04) READ MORE
normal 2003-02-01 EA-4/14 INF Selection and use of reference materials READ MORE
normal 2018-11-28 READ MORE
Status Date Reference Description
new 2023-11-08 EA Code of Conduct READ MORE
Status Date Reference Description
revised 2024-03-15 EA-INF/02 Contact Persons of EA Members, Recognized Stakeholders and Observers READ MORE
revised 2024-03-15 EA-INF/01 List of EA Publications and International Documents READ MORE
revised 2024-02-19 EA-1/15 A EA policy for relations with stakeholders READ MORE
revised 2024-01-22 EA-INF/03 Signatories to the EA Multilateral Agreement READ MORE
revised 2024-01-18 EA-INF/05 Directory of European legislations and EU schemes with provisions to accreditation and/or conformity assessment READ MORE
revised 2023-11-28 EA-INF/17 Register of EA resolutions for use by EA, National Accreditation Bodies and EA evaluators READ MORE
revised 2023-11-20 EA-2/15 M EA requirements for the accreditation of flexible scopes READ MORE

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Our mission is to ensure confidence in accredited conformity assessments results through harmonized operation of accreditation activities in support of European and global economies.

Accreditation
for Regulators

Accreditation operates in the public interest across all market sectors. It provides an attestation that accredited bodies offering testing, examination, calibration, certification, inspection and verification services have the technical competence and impartiality to check the conformity of products and services with the relevant standards and regulations.

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Accreditation
for Industry/Economy

Accreditation is a third party, impartial and independent process to assess that an organization is competent to perform specific tests, inspections, measurements and certifications. By using accredited services, businesses can demonstrate compliance with standards and regulations. Accreditation provides confidence in certificates and conformity attestations.

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Accreditation
for Conformity
Assessment Bodies

Accreditation determines the technical competence, integrity and impartiality of organizations providing conformity assessment services such as testing, calibration, certification, and inspection based on international standards. Accreditation is an impartial and objective process that provides the least duplicative, the most transparent…

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Accreditation
for Consumers/Citizens

Consumers want to have confidence in the goods and services they buy and use. Accreditation exists to give that confidence. How is this possible ? Products are manufactured and food is supplied in conformity with specific quality, security or safety requirements. Laboratories or certifiers check and confirm that conformity.

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