BS EN ISO/IEC 17025:2017
Current
The latest, up-to-date edition.
General requirements for the competence of testing and calibration laboratories
Hardcopy , PDF
English
25-06-2018
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Structural requirements
6 Resource requirements
7 Process requirements
8 Management system requirements
Annex A (informative) - Metrological traceability
Annex B (informative) - Management system options
Bibliography
Defines the general requirements for the competence, impartiality and consistent operation of laboratories.
| Committee |
CAS/1
|
| DevelopmentNote |
Supersedes BS 7501(1989) and 98/402556 DC. (04/2000) Supersedes 03/317065 DC. (07/2005) Supersedes 17/30315164 DC. (12/2017)
|
| DocumentType |
Standard
|
| ISBN |
9780539014143
|
| Pages |
40
|
| PublisherName |
British Standards Institution
|
| Status |
Current
|
| Supersedes |
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.
| Standards | Relationship |
| I.S. EN ISO/IEC 17025:2005 | Identical |
| ISO/IEC 17025:2017 | Identical |
| NBN EN ISO/IEC 17025 : 2005 COR 2006 | Identical |
| ISO/IEC 17025:2005 | Identical |
| EN ISO/IEC 17025:2017 | Identical |
| UNE-EN ISO/IEC 17025:2017 | Equivalent |
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| 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 |
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| 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 |
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| 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 |
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| ISO 5725-6:1994 | Accuracy (trueness and precision) of measurement methods and results — Part 6: Use in practice of accuracy values |
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| 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 |
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| 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 |
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| ISO/IEC Guide 98-3:2008 | Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995) |
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