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DIN Standards Committee Health Technologies

DIN EN ISO 15189 [Withdrawn] references following documents:

Document number Edition Title
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 17034 2016-11 General requirements for the competence of reference material producers More 
ISO 17511 2020-04 In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples More 
ISO 18113-1 2022-10 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements More 
ISO 20166-1 2018-12 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA More 
ISO 20166-2 2018-12 Molecular in vitro diagnostic examinations - Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 2: Isolated proteins More