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| 文 件
名 称 |
文件编号 |
| 定量测定室内质量控制检验:原理和定义 |
C24-A2 |
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| 临床化学设备性能的精密度评价;建议指南 |
EP5-T2 |
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临床化学设备操作精密度评价
核准指南
(
Evaluation of Precision Performance of Clinical Chemistry Devices; Approved
Guideline ) |
EP5-A |
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| 定量分析方法的线性评估;暂定指南 |
EP6-P |
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定量分析方法的线性评价:统计方法,提议指南第二版(
Evaluation of the Linearity of Quantitative Analytical Methods: A
Statistical Approach; Proposed Guideline Second Edition
) |
EP6-P2 |
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| 临床化学干扰试验;建议指南(
Interference Testing in Clinical Chemistry; Proposed Guideline
) |
EP7-P |
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| 用患者样本进行方法对比及偏差评估—批准指南(
Method Comparison and Bias Estimation Using Patient Samples; Approved
Guideline )(1995) |
EP9-A |
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定量临床实验室方法的初步评价,核准指南(
Preliminary Evaluation of Quantitative Clinical Laboratory Methods; Approved
Guideline ) |
EP10-A |
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| 应用ROC曲线图评价实验室检验项目的临床准确性的指导原则 |
GP10-A |
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用于体外诊断检验说明的统一描述,提议指南( Uniform Description of Claims For In Vitro Diagnostic Tests;
Proposed Guideline ) |
EP11-P |
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用于定性实验评价的用户协议,提议指南( User Protocol for Evaluation of Qualitative Test Performance;
Proposed Guideline ) |
EP12-P |
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实验室统计—标准差,报告
(
Laboratory Statistics — Standard Deviation; A Report
) |
EP13-R |
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基质效应的评价,核准指南
(
Evaluation of Matrix Effects; Approved Guideline
) |
EP14-A |
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精密度和准确度性能的应用,核准指南(
User Demonstration of Performance for Precision and Accuracy; Approved
Guideline ) |
EP15-A |
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检验单位使用的质量管理,提议指南(
Quality Management for Unit-Use Testing; Proposed Guideline
) |
EP18-P |
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临床实验方法 总分析 误差的评估,提议指南(
Estimation of Total Analytical Error for Clinical Laboratory Methods;
Proposed Guideline )
|
EP21-P |
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| 抗微生物药物敏感试验纸片法的执行标准-第6版;已批准的标准(1997) |
M2-A6 |
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| 为空气条件下可生长的细菌设计的抗微生物药敏感试验稀释法-第4版;已批准的标准(1997) |
M7-A4 |
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| 抗微生物药物敏感试验的执行标准;第9版信息增刊(1999) |
M100-S9 |