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BS EN ISO 16256:2021 - TC

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Tracked Changes. Clinical laboratory testing and in vitro diagnostic test systems. Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases

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Related Information

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  • BS EN 13532:2002

    General requirements for in vitro diagnostic medical devices for self-testing

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    Elimination or reduction of risk of infection related to in vitro diagnostic reagents

  • BS EN 13975:2003

    Sampling procedures used for acceptance testing of in vitro diagnostic medical devices. Statistical aspects

  • BS EN 14136:2004

    Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures

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BS EN ISO 16256:2021 - TC

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