• The placement of QC samples should be judiciously considered in the run.

    QC样品的位置,应在运行中明智而谨慎的考虑。

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  • The number of QC samples to ensure proper control of the assay should be determined based on the run size.

    确保适当分析控制的QC样品的数量应根据运行量证明。

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  • Complete serial chromatograms from 5-20% of subjects, with standards and QC samples from those analytical runs.

    从分析批中5- 20%课题的有标准品和QC样品的完整的一系列色谱图。

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  • We recommend that these samples span a level of positivity with QC samples having a known negative, low, medium, and high reactivity in the assay.

    我们推荐这些样品的阳性度水平应涵盖检测使用的已知反应性(无、低、中以及高反应性)质控样品相应的水平。

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  • This can be accomplished by analysis of replicate sets of analyte samples of known concentrations QC samples from an equivalent biological matrix.

    这可以用重复分析一系列相等的生物基质中已知浓度的QC样品来完成。

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  • Does factory QC compare first piece samples with approval sample and specification sheet?

    工厂QC是否根据客户签样和产品规格表来制定首件样品?

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  • Does factory QC compare first piece samples with approval sample and specification sheet?

    工厂QC是否针对批准样板和规格书对比首件样板?

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  • Does factory QC compare first piece samples with approval sample and specification sheet?

    工厂QC是否比较首件样品抽样检验和批准的规格表?

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  • We need to submit two each additional samples for QC approval.

    我们需要每种样品再增加两个,以供质量控制部门确认。

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  • Methods 29 strains from QC stains clinical samples and were identified by ATB Expression and manual method.

    方法用ATB细菌鉴定仪与手工法分别鉴定29株来自质控及临床标本菌株。

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  • Methods 29 strains from QC stains clinical samples and were identified by ATB Expression and manual method.

    方法用ATB细菌鉴定仪与手工法分别鉴定29株来自质控及临床标本菌株。

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