NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 15189 [Withdrawn] references following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN EN ISO 9000 | 2015-11 | Quality management systems - Fundamentals and vocabulary (ISO 9000:2015); German and English version EN ISO 9000:2015 More |
| DIN EN ISO 9001 | 2015-11 | Quality management systems - Requirements (ISO 9001:2015); German and English version EN ISO 9001:2015 More |
| DIN EN ISO/IEC 17000 | 2020-09 | Conformity assessment - Vocabulary and general principles (ISO/IEC 17000:2020); Trilingual version EN ISO/IEC 17000:2020 More |
| DIN EN ISO/IEC 17011 | 2018-03 | Conformity assessment - Requirements for accreditation bodies accrediting conformity assessment bodies (ISO/IEC 17011:2017); German and English version EN ISO/IEC 17011:2017 More |
| DIN EN ISO/IEC 17021-1 | 2015-11 | Conformity assessment - Requirements for bodies providing audit and certification of management systems - Part 1: Requirements (ISO/IEC 17021-1:2015); German and English version EN ISO/IEC 17021-1:2015 More |
| DIN EN ISO/IEC 17025 | 2018-03 | General requirements for the competence of testing and calibration laboratories (ISO/IEC 17025:2017); German and English version EN ISO/IEC 17025:2017 More |
| ISO 15190 | 2020-02 | Medical laboratories - Requirements for safety More |
| ISO 15194 | 2009-05 | In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation More |
| ISO 15198 | 2004-07 | Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer More |
| ISO 17034 | 2016-11 | General requirements for the competence of reference material producers More |
