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The CLIA-88 regulations for calibration verfication state that calibration verification is required:
Once every six months
When you see a drift in your daily quality control results
After a major preventive maintenance or replacement of a critical part
All of the above
Only A and C
Which of the following does CLIA define as acceptable calibration verification material:
Any patient samples
Pooled serum
A solution that has a known amount of a specific analyte
All of the above
Which of the following assays do not require routine calibration verification:
Prothrombin time
Free T3 and/or Free T4
Urine Magnesium
Only A and C
All of the above
If your analyzer performs a 3 point calibration, are you required to perform calibration verification?
Yes
No
Only if your analyzer performs this calibration at least once every six months
CLIA requires that you run calibration verification using:
A zero or minimal value at or near the lower limit of the instrument's reportable range
A mid-point value
A maximum value at or near the upper limit of the instrument's reportable range
A minimum of 3 points anywhere within the instrument's reportable range
Only A, B and C