UNE-EN ISO/IEC 17025:2017
Current
The latest, up-to-date edition.
General requirements for the competence of testing and calibration laboratories (ISO/IEC 17025:2017)
Hardcopy , PDF
Spanish, Castilian, English, Catalan
20-12-2017
1.1 This International Standard specifies the general requirements for the competence, impartiality and consistent operation of laboratories as defined in the standard.1.2 This International Standard is applicable to all organizations, regardless of the number of personnel, performing laboratory activities (see 3.6) .1.3 Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others can also use this International Standard in confirming or recognizing the competence of laboratories.
| Committee |
CTN 66/SC 2
|
| DevelopmentNote |
Supersedes UNE 66501 and UNE 66800. (09/2003)
|
| DocumentType |
Standard
|
| Pages |
44
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Current
|
| Standards | Relationship |
| EN ISO/IEC 17025:2017 | Identical |
| BS EN ISO/IEC 17025:2005 | Identical |
| I.S. EN ISO/IEC 17025:2005 | Identical |
| ISO/IEC 17025:2017 | Identical |
| NBN EN ISO/IEC 17025 : 2005 COR 2006 | Identical |
| ISO/IEC 17065:2012 | Conformity assessment — Requirements for bodies certifying products, processes and services |
| ISO/IEC 17000:2004 | Conformity assessment — Vocabulary and general principles |
| ISO 5725-1:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 1: General principles and definitions |
| ISO 17034:2016 | General requirements for the competence of reference material producers |
| ISO 19011:2011 | Guidelines for auditing management systems |
| ISO 15194:2009 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation |
| ISO 15189:2012 | Medical laboratories — Requirements for quality and competence |
| ISO 31000:2009 | Risk management — Principles and guidelines |
| ISO/IEC Guide 98-4:2012 | Uncertainty of measurement — Part 4: Role of measurement uncertainty in conformity assessment |
| ISO 5725-3:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 3: Intermediate measures of the precision of a standard measurement method |
| ISO Guide 33:2015 | Reference materials — Good practice in using reference materials |
| ISO 5725-6:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 6: Use in practice of accuracy values |
| ISO Guide 35:2017 | Reference materials — Guidance for characterization and assessment of homogeneity and stability |
| ISO 5725-4:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 4: Basic methods for the determination of the trueness of a standard measurement method |
| ISO/IEC 17011:2004 | Conformity assessment — General requirements for accreditation bodies accrediting conformity assessment bodies |
| ISO Guide 80:2014 | Guidance for the in-house preparation of quality control materials (QCMs) |
| ISO/IEC Guide 99:2007 | International vocabulary of metrology — Basic and general concepts and associated terms (VIM) |
| ISO 17511:2003 | In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materials |
| ISO/IEC 17020:2012 | Conformity assessment — Requirements for the operation of various types of bodies performing inspection |
| ISO/IEC 17043:2010 | Conformity assessment — General requirements for proficiency testing |
| ISO Guide 30:2015 | Reference materials — Selected terms and definitions |
| IEC GUIDE 115:2007 | Application of uncertainty of measurement to conformity assessment activities in the electrotechnical sector |
| ISO/IEC 12207:2008 | Systems and software engineering — Software life cycle processes |
| ISO 10012:2003 | Measurement management systems — Requirements for measurement processes and measuring equipment |
| ISO 5725-2:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 2: Basic method for the determination of repeatability and reproducibility of a standard measurement method |
| ISO 9001:2015 | Quality management systems — Requirements |
| ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
| ISO 21748:2017 | Guidance for the use of repeatability, reproducibility and trueness estimates in measurement uncertainty evaluation |
| ISO Guide 31:2015 | Reference materials — Contents of certificates, labels and accompanying documentation |
| OIML V 1 : 2013 | INTERNATIONAL VOCABULARY OF TERMS IN LEGAL METROLOGY (VIML) |
| ISO/IEC Guide 98-3:2008 | Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995) |
| ISO/IEC 17021-1:2015 | Conformity assessment — Requirements for bodies providing audit and certification of management systems — Part 1: Requirements |
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