EN ISO 17034:2016
Current
The latest, up-to-date edition.
General requirements for the competence of reference material producers (ISO 17034:2016)
30-11-2016
European foreword
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Structural requirements
6 Resource requirements
7 Technical and production requirements
8 Management system requirements
Annex A (informative) - Summary of production
requirements for RMs and CRMs
Bibliography
ISO 17034:2016 specifies general requirements for the competence and consistent operation of reference material producers.ISO 17034:2016 sets out the requirements in accordance with which reference materials are produced. It is intended to be used as part of the general quality assurance procedures of the reference material producer.ISO 17034:2016 covers the production of all reference materials, including certified reference materials.
| Committee |
CEN/CLC/JTC 1
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| UNI CEI EN ISO 17034 : 2017 | Identical |
| PN EN ISO 17034 : 2017 | Identical |
| NS EN ISO 17034 : 2016 | Identical |
| NEN-EN-ISO 17034:2016 | Identical |
| NF EN ISO 17034 : 2016 | Identical |
| ISO 17034:2016 | Identical |
| BS EN ISO 17034:2016 | Identical |
| DIN EN ISO 17034:2015-12 (Draft) | Identical |
| SN EN ISO 17034 : 2017 | Identical |
| I.S. EN ISO 17034:2016 | Identical |
| UNE-EN ISO 17034:2017 | Identical |
| DIN EN ISO 17034:2017-04 | Identical |
| SS-EN ISO 17034:2016 | Identical |
| CEI UNI EN ISO 17034 : 1ED 2018 | Identical |
| ISO/IEC 17025:2005 | General requirements for the competence of testing and calibration laboratories |
| ISO/IEC 17000:2004 | Conformity assessment Vocabulary and general principles |
| ISO 15195:2003 | Laboratory medicine Requirements for reference measurement laboratories |
| 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/TR 16476:2016 | Reference materials — Establishing and expressing metrological traceability of quantity values assigned to reference materials |
| ISO Guide 35:2017 | Reference materials — Guidance for characterization and assessment of homogeneity and stability |
| ISO/IEC 17011:2004 | Conformity assessment General requirements for accreditation bodies accrediting conformity assessment bodies |
| ISO/IEC Guide 99:2007 | International vocabulary of metrology Basic and general concepts and associated terms (VIM) |
| ISO Guide 30:2015 | Reference materials — Selected terms and definitions |
| ISO 10012:2003 | Measurement management systems — Requirements for measurement processes and measuring equipment |
| ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
| ISO Guide 31:2015 | Reference materials — Contents of certificates, labels and accompanying documentation |
| ECA ILAC P10 : 2013 | ILAC POLICY ON TRACEABILITY OF MEASUREMENT RESULTS |
| ISO/IEC Guide 98-3:2008 | Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995) |
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.