ICS:11.100.10
Showing 10–18 of 37 results
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ISO 18113:2022 In vitro diagnostic medical devices – Information supplied by the manufacturer (labelling) – Part 2: In vitro diagnostic reagents for professional use
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ISO 15193:2009 In vitro diagnostic medical devices – Measurement of quantities in samples of biological origin – Requirements for content and presentation of reference measurement procedures
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ISO 13079:2011 Laboratory glass and plastics ware – Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method
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ISO 4307:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for saliva – Isolated human DNA
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ISO 21474:2024 In vitro diagnostic medical devices – Multiplex molecular testing for nucleic acids – Part 3: Interpretation and reports
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ISO 16766:2024 Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergency
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ISO 20166:2018 Molecular in vitro diagnostic examinations – Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue – Part 2: Isolated proteins
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ISO 20184:2018 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for frozen tissue – Part 2: Isolated proteins
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ISO 21151:2020 In vitro diagnostic medical devices – Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples
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