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11.100.10 Systémy diagnostických zkoušek in vitro

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BS EN ISO 20166-2:2018
Molecular in vitro diagnostic examinations. Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue Isolated proteins

Vydáno: 2019-01-04

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BS EN 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

Vydáno: 2016-01-31

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BS EN 14136:2004
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures

Vydáno: 2004-05-26

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BS EN ISO 15197:2015 - TC
Tracked Changes. In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

Vydáno: 2020-02-25

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BS ISO 21151:2020
In vitro diagnostic medical devices. Requirements for international harmonisation protocols establishing metrological traceability of values assigned to calibrators and human samples

Vydáno: 2020-05-27

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BS EN ISO 6717:2021
In vitro diagnostic medical devices. Single-use containers for the collection of specimens from humans other than blood

Vydáno: 2021-09-08

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BS EN ISO 23118:2021 - TC
Tracked Changes. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma

Vydáno: 2022-01-27

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24/30463896 DC
BS EN ISO 18704 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA

Vydáno: 2024-10-23

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BS EN ISO 20916:2024
In vitro diagnostic medical devices. Clinical performance studies using specimens from human subjects. Good study practice

Vydáno: 2024-07-31

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BS EN ISO 18113-2:2024 - TC
Tracked Changes. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) In vitro diagnostic reagents for professional use

Vydáno: 2024-06-14

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BS EN ISO 18113-2:2024
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) In vitro diagnostic reagents for professional use

Vydáno: 2024-06-12

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BS EN ISO 18113-5:2024 - TC
Tracked Changes. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) In vitro diagnostic instruments for self-testing

Vydáno: 2024-06-14

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76 results

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