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WorksheetsISO/IEC 17025:2017 LMS Requirements (Part 2)
Total questions: 10
Worksheet time: 4mins
The lab personnel review the test request to confirm the belows. (Multiple answers)
Available of competent personnel to conduct the test.
Available of equipment and required chemicals/ reagent to perform the test.
Test method used is suitable and compatible for type of sample matrix received.
Opportunity to expand the business territory.
Methodologies for method validation. (Multiple answers)
Selectivity and specificity
Repeatability of test
Reproducibility of test such as proficiency testing and interlab comparison
Spiked sample and recovery test
Purposes of sample identification and labeling/ marked? (Multiple answers)
Unique to the specific test item only.
Traceble from the test item itself to its applicable analysis worksheet, logbook and Test Report.
Nice design
When a data or test result is wrongly written...
Erase it
Use correction pen to correct it
Cross it, then the correct data/ value entered alongside and initialed by the person making the correction
Why we need to duplicate / replicate the testing? (Multiple answers)
Enhance result confident.
Detect outliers
More result options
Justify whether to accept or reject the test result or repeat the testing
Purposes of Quality Control (QC) Chart. (Multiple answers)
To monitor the trend of test result (result distributions)
To monitor the test result obtained whether within the acceptance criteria (mean + 2SD and mean - 2SD)
For record and drawing purposes
What is Proficiency Testing (PT)?
Same batch of test item distributed to all participated laboratories to carry out the testing within the same period
Result comparison within the participated laboratories
Result evaluation whether within the satisfactory range / z-score
Indicate laboratory's overall performance, equipment performance, test performance and personnel performance
The laboratory shall keep the technical records for a minimum of ...
3 years
7 years
6 years
5 years
Document control procedure consists of... (Multiple answers)
Review and approve prior distributed
Identified with document title, document number, revision number and effective date
Retained obsolete copy are suitable marked with "OBSOLETE"
Document Master List to overview the availbility of documents and its current revision status
Outputs from internal audit... (Multiple answers)
Audit plan / schedule
Report of audit findings, evidence and observation
Non-Conformity Report (NCR)
