Analyse-it® Method Evaluation Edition
Validate, verify, or demonstrate method precision over the reportable range, to
satisify CLSI EP5 and meet FDA method validation requirements.
Simple single-run precision is provided for a quick precision check. For in-depth analysis CLSI EP5 is supported
to examine precision within a single run, precision between runs (for example morning
and afternoon), precision over a number of days, and precision over the reportable
range (often near the upper and lower) of analyte concentrations.
- Determine a simple precision estimate
Calculate SD or CV(%) precision from a single run.
- Determine total precision & repeatability
Satisifies CLSI EP5-A2. Calculates Total precision (within-device/laboratory) and
Repeatability (within-run) SD or CV(%) from 1- or 2- runs over many days, or over
a range of analyte concentrations.
- Demonstrate precision is within allowable goal or meets manufacturer's claim
Satisfies CLSI EP5-A2 & EP15-A2. Express allowable precision as absolute/percentage of concentration,
or as Random Error% of Total Allowable Error (TAe).
- Visually assess precision
A precision plot shows the scatter of observations.
What next?
Download a free 30-day evaluation