Questions and Answers
What is the purpose of inter-laboratory comparisons and other performance evaluations?
To determine the individual and collective laboratory performance characteristics
What is the main purpose of the EQAS program?
To compare laboratory results with those of other laboratories
Why were PT/EQA programs introduced into laboratory medicine more than 60 years ago?
To address differences in results for aliquots of the same sample measured by different laboratories
What does EQAS stand for in the context of laboratory quality management?
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What is the primary focus of an EQAS for Pre Analytical?
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Which statement best describes the role of inter-laboratory comparisons in laboratory quality management?
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In the context of a PT/EQA program, what is the significance of traceable reference values?
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What is an ideal characteristic of samples for a PT/EQA program?
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What should laboratories do upon receiving the specimen package for a PT/EQA program?
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What is an important consideration when handling high, out-of-range samples in a PT/EQA program?
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What happens if a laboratory submits results for PT/EQA samples after the Sample Due Date?
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What does the organizer include in the report of a PT/EQA program?
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Why should PT/EQA samples be handled as patient samples?
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What is an important consideration when selecting a PT provider for a laboratory?
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What should laboratories do while handling lyophilized PT/EQA samples?
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What should laboratories ensure regarding configuration codes in a PT/EQA program?
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What does the PT/EQA organizer evaluate regarding laboratory performance?
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In the context of laboratory quality management, what is the primary purpose of an inter-laboratory comparison?
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What is the main objective of an External Quality Assessment (EQA) program in laboratory medicine?
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What is a fundamental characteristic of Pre Analytical EQAS samples for laboratory testing?
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What is the significance of traceable reference values in the context of a PT/EQA program?
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Why were PT/EQA programs introduced into laboratory medicine more than 60 years ago?
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What role do inter-laboratory comparisons play in improving the overall quality management of laboratory testing?
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In a PT/EQA program, what characteristic should the ideal samples fulfill?
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What is a key consideration when selecting a PT provider for a laboratory in the context of EQA programs?
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What should laboratories ensure regarding configuration codes in a PT/EQA program?
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Why is it important to handle high, out-of-range samples in accordance with established laboratory procedures in a PT/EQA program?
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What happens if a laboratory submits results for each specimen after the Sample Due Date in a PT/EQA program?
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What is the role of inter-laboratory comparisons in laboratory quality management?
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What should laboratories do upon receiving the specimen package for a PT/EQA program?
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Why are traceable reference values important in the context of PT/EQA programs?
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What is an ideal characteristic of PT/EQA samples?
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What does the PT/EQA organizer evaluate regarding laboratory performance?
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What should laboratories do while handling lyophilized PT/EQA samples?
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