PD ISO Guide 34:2009
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
General requirements for the competence of reference material producers
Hardcopy , PDF
30-11-2016
English
31-01-2010
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Organization and management requirements
5 Technical and production requirements
Annex A (informative) - Metrological traceability of
certified property values of reference
materials
Annex B (informative) - Commutability of reference
materials
Annex C (informative) - ISO/IEC 17025/ISO Guide 34
cross-reference table
Bibliography
Describes general requirements in accordance with which a reference material producer has demonstrate that it operates, if it is to be recognized as competent to carry out the production of reference materials.
| Committee |
RMI/1
|
| DevelopmentNote |
Supersedes BS PD6532-5(2000). (01/2010)
|
| DocumentType |
Standard
|
| Pages |
46
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO Guide 34:2009 | 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 Guide 32:1997 | Calibration in analytical chemistry and use of certified reference materials |
| CLSI EP14 A2 : 2ED 2005 | EVALUATION OF MATRIX EFFECTS |
| ISO 15189:2012 | Medical laboratories — Requirements for quality and competence |
| ISO Guide 33:2015 | Reference materials — Good practice in using reference materials |
| ISO Guide 35:2017 | Reference materials — Guidance for characterization and assessment of homogeneity and stability |
| 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 3534-2:2006 | Statistics — Vocabulary and symbols — Part 2: Applied statistics |
| ISO Guide 30:2015 | Reference materials — Selected terms and definitions |
| CLSI EP32 R : 1ED 2006 | METROLOGICAL TRACEABILITY AND ITS IMPLEMENTATION |
| ISO 10012:2003 | Measurement management systems — Requirements for measurement processes and measuring equipment |
| ISO 9001:2015 | Quality management systems — Requirements |
| CLSI C53 P : 1ED 2008 | CHARACTERIZATION AND QUALIFICATION OF COMMUTABLE REFERENCE MATERIALS FOR LABORATORY MEDICINE |
| ISO 9000:2015 | Quality management systems — Fundamentals and vocabulary |
| ECA ILAC G12 : 2000 | GUIDELINES FOR THE REQUIREMENTS FOR THE COMPETENCE OF REFERENCE MATERIALS PRODUCERS |
| ISO Guide 31:2015 | Reference materials — Contents of certificates, labels and accompanying documentation |
| ECA ILAC G24 : 2007 | GUIDELINES FOR THE DETERMINATION OF CALIBRATION INTERVALS OF MEASURING INSTRUMENTS |
| ECA ILAC P10 : 2013 | ILAC POLICY ON TRACEABILITY OF MEASUREMENT RESULTS |
| OIML D 10 : 2007 | GUIDELINES FOR THE DETERMINATION OF CALIBRATION INTERVALS OF MEASURING INSTRUMENTS |
| ISO/IEC Guide 98-3:2008 | Uncertainty of measurement — Part 3: Guide to the expression of uncertainty in measurement (GUM:1995) |
| ISO 3534-1:2006 | Statistics — Vocabulary and symbols — Part 1: General statistical terms and terms used in probability |
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