Ghiduri
Documente generale
- EA-1/22:2020 - EA Procedure and Criteria for the Evaluation of Conformity Assessment Schemes by EA Accreditation Body Members
- EA-2/13 M:2019 - EA Cross Border Accreditation Policy and Procedure for Cross Border Cooperation between EA Members ☛ traducerea în limba română
- EA-2/20 G:2020 - Consultancy, and the Independence of Conformity Assessment Bodies
- EA-INF/05:2023 - Directory of European legislations and EU schemes with provisions to accreditation and/or conformity assessment
- IAF MD 7:2010 - Harmonisation of Sanctions ☛ traducerea în limba română
- IAF MD 7:2023 - IAF Mandatory Document for the Harmonization of Sanctions and Dealing with Fraudulent Behaviour
- IAF ID 15:2023 - Dealing with Fraudulent Behaviour
- IAF MD 25:2022 - Criteria for evaluation of conformity assessment schemes ☛ traducerea în limba română
Laboratoare
- EA-4/02 M:2022 - Evaluation of the Uncertainty of Measurement in Calibration
- EA-4/09 G:2022 - Accreditation for sensory testing laboratories
- EA-4/14 INF:2003 - The Selection and Use of Reference Materials ☛ traducerea în limba română
- EA-4/17 M:2022 - Description of scopes of accreditation for medical laboratories
- EA-4/18 G:2021 - Guidance on the level and frequency of proficiency testing participation
- EA-4/22 G:2018 - EA Guidance on Accreditation of Pesticide Residues Analysis in Food and Feed
- ILAC G8:09/2019 - Guidelines on Decision Rules and Statements of Conformity
- ILAC G17:10/2021 - Introducing the Concept of Uncertainty of Measurement in Testing
- ILAC-G18:12/2021 - Guideline for describing Scopes of Accreditation
- ILAC G19:06/2022 - Modules in a Forensic Science Process
- ILAC G24:2022 - Guidelines for the determination of calibration intervals of measuring equipment
- ILAC G26:2018 - Guidance for the Implementation of a Medical Accreditation Scheme
- ILAC P9:06/2014 - ILAC Policy for Participation in Proficiency Testing Activities ☛ traducerea în limba română
- ILAC P10:07/2020 - ILAC Policy on Metrological Traceability of Measurement Results ☛ traducerea în limba română
- ILAC P14:09/2020 - ILAC Policy for Uncertainty in Calibration ☛ traducerea în limba română
Furnizori de încercări de competenţă
Inspecţie
- ILAC P15:05/2020 - Application of ISO/IEC 17020:2012 for the Accreditation of Inspection Bodies ☛ traducerea în limba română
- ILAC G19:06/2022 - Modules in a Forensic Science Process
- ILAC G27:07/2019 - Guidance on measurements performed as part of an inspection process
- ILAC G28:07/2018 - Guideline for the Formulation of Scopes of Accreditation for Inspection Bodies
Certificare
- EA-2/17 M:2020 - EA Document on Accreditation for Notification Purposes ☛ traducerea în limba română
- EA-3/02 M:2022 - EA policy for the accreditation of Certification Bodies providing certification of PDO, PGI and TSG
- EA-3/12 M:2022 - EA Policy for the Accreditation of Organic Production Certification, 9th March 2022_rev02 - ☛ traducerea în limba română
- EA-7/04 M:2017 - Legal Compliance as a part of accredited ISO 14001: 2015 certification
- IAF ID 1:2020 - IAF Informative Document for QMS and EMS Scopes of Accreditation
- IAF ID 3:2011 - Informative Document for Management of Extraordinary Events or Circumstances Affecting ABs, CABs and Certified Organizations ☛ traducerea în limba română
- IAF MD 1:2018 - IAF Mandatory Document for the Audit and Certification of a Management System Operated by a Multi-Site Organization
- IAF MD 2:2017 - IAF Mandatory Document for the Transfer of Accredited Certification of Management Systems ☛ traducerea în limba română
- IAF MD 4:2022 - IAF Mandatory Document for the Use of Information and Communication Technology (ICT) for Auditing/Assessment Purposes (Issue 2, Version 3)
- IAF MD 5:2019 Determination of audit time of Quality, Environmental, and Occupational Health & Safety Management Systems ☛ traducerea în limba română
- IAF MD 9:2017 - Application of ISO/IEC 17021-1 in the Field of Medical Device Quality Management Systems (ISO 13485)
- IAF MD 9:2022 - Application of ISO/IEC 17021-1 in the Field of Medical Device Quality Management Systems (ISO 13485) (Issue 4)
- IAF MD 11:2013 - IAF mandatory document for the application of ISO/IEC 17021-1 for audits of integrated management systems ☛ traducerea în limba română
- IAF MD 12:2016 - Accreditation Assessment of Conformity Assessment Bodies with Activities in Multiple Countries ☛ traducerea în limba română
- IAF MD 13:2022 - Knowledge Requirements for Accreditation Body Personnel for Information Security Management Systems (ISO/IEC 27001)
- IAF MD 15:2014 - IAF Mandatory Document for the Collection of Data to Provide Indicators of MS CB’ Performance ☛ traducerea în limba română
- IAF MD 17:2019 - Witnessing activities for the accreditation of management systems certification bodies ☛ traducerea în limba română
- IAF MD 21:2022 - Requirements for the Migration to ISO 45001:2018 from OHSAS 18001:2007 (Issue 1, Version 3)
- IAF MD 22:2019 - Application of ISO/IEC 17021-1 for the Certification of Occupational Health and Safety Management Systems (OH&SMS) ☛ traducerea în limba română
- IAF MD 23:2018 - Control of Entities Operating on Behalf of Accredited Management Systems Certification Bodies
- IAF MD 24:2021 - Transition Requirements for ISO 50003:2021 ☛ traducerea în limba română
- IAF MD 26:2023 - Transition requirements for ISO/IEC 27001:2022, Issue 2 ☛ traducerea în limba română
Verificare GES
- EA-6/03 M:2022 - EA document for recognition of verifiers under EU ETS Directive
- IAF MD 6:2014 - Application of ISO 14065:2013 ☛ traducerea în limba română