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共找到 150 條與 參考測(cè)量程序 相關(guān)的標(biāo)準(zhǔn),共 10 頁(yè)

本標(biāo)準(zhǔn)用于血清中總蛋白含量的測(cè)量

Reference measurement procedure of total protein in serum

本標(biāo)準(zhǔn)規(guī)定了血清膽固醇參考測(cè)量程序(分光光度法)及其質(zhì)量保證的基本原則。 本標(biāo)準(zhǔn)適用于從事血脂研究的實(shí)驗(yàn)室或血脂參考實(shí)驗(yàn)室測(cè)定膽固醇

Reference measurement procedure for serum cholesterol.Spectrophotometry

The document is applicable to determination of batroxobin time in plasma from citrated venous blood. Most fibrin polymerisation disorders increase

Haemostaseology - Reference measurement procedure for the determination of batroxobin time

In vitro diagnostic medical devices — Requirements for reference measurement procedures

Haemostaseology - Reference measurement procedure for the determination of batroxobin time

Serum cholesterol reference measurement procedure spectrophotometry (obsolete)

Serum Electrolytes (Potassium, Sodium, Calcium, Magnesium) Reference Measurement Procedure (Ion Chromatography)

1???Scope This document specifies the photometric reference measurement procedure for the determination of volume of piston-operated

Piston-operated volumetric apparatus - Photometric reference measurement procedure for the determination of volume

BS EN ISO 15193 In vitro diagnostic medical devices - Requirements for reference measurement procedures

In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/DIS 15193:2023)

In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/DIS 15193:2023); German and English version prEN ISO 15193:2023 / Note: Date of issue 2024-01-05*Intended as replacement for DIN EN ISO 15193 (2009-10).

本標(biāo)準(zhǔn)規(guī)定了在臨床醫(yī)學(xué)應(yīng)用中,測(cè)量天門冬氨酸氨基轉(zhuǎn)移酶催化活性濃度的參考測(cè)量程序。 本標(biāo)準(zhǔn)主要適用于參考實(shí)驗(yàn)室,作為天門冬氨酸氨基轉(zhuǎn)移酶催化活性濃度測(cè)量的溯源,也可作為與 酶催化活性濃度檢驗(yàn)有關(guān)的儀器和試劑生產(chǎn)企業(yè)的溯源,可供有關(guān)認(rèn)可監(jiān)督管理單位及質(zhì)量管理部門應(yīng) 用。此參考測(cè)量程序可用于我國(guó)臨床常規(guī)

Aspartate aminotransferase catalytic activity concentration reference measurement procedure

Draft Document - In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/DIS 15193:2023); German and English version prEN ISO 15193:2023

Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018); German version EN ISO 15195:2019

本文件規(guī)定了醫(yī)學(xué)校準(zhǔn)實(shí)驗(yàn)室運(yùn)行參考測(cè)量程序的能力要求。 本文件以GB/T27025—2019 的要求為規(guī)范性參考,列出了校準(zhǔn)實(shí)驗(yàn)室充分執(zhí)行任務(wù)的附加要求。 本文件與GB/T27025—2019 條款的關(guān)系總結(jié)于附錄A中。 本文件不包括以名義標(biāo)度或序數(shù)標(biāo)度報(bào)告結(jié)果的特性的測(cè)量。 本文件不適用于醫(yī)學(xué)

Laboratory medicine—Requirements for the competence of calibration laboratories using reference measurement procedures




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