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BS EN 928:1996

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Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices

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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 928:1996

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