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32 Cards in this Set

  • Front
  • Back
Quality Assurance
Quantitative indications that indicate whether data requirements have been met. Also refers to the broader process that includes quality control, quality assessment, and documentation os procedures and results designed to ensure adequate data quality.
Use Objective
States the purpose for which results will be used
Specifications
describes how good analytical results need to be and what precautions are required in an analytical method
False Positive
conclusion that a concentration of analyte exceeds a certain limit when, in fact, the concentration is below the limit
False Negative
conclusion that a concentration of analyte is below a certain limit when, in fact, the concentration is above the limit
Selectivity
being able to distinguish analyte from other species in the sample
Sensitivity
the capability of responding reliably and measurably to changes in analyte concentration (slope of the calibration curve)
Method Blank
a sample containing all components except analyte and is taken through all steps of the analytical process (response is subtracted from samples response)
Reagent Blank
a solution prepared from all of the reagents, but with no analyte (measures the response of the analytical method to impurities in the reagents and other effects caused by any component other than analyte)
Field Blank
blank sample exposed to the environment at the sample collection site and transported in the same manner as other samples between the lab and the field
Matrix
everything in the sample other than analyte
Spike
addition of a known compound (usually with known concentration) to an unknown
Calibration Check
the analysis of a solution formulated by the analyst to contain a known concentration of analyte
Performance Test Samples
it is inserted in a series of measurements to see if a procedure gives correct results when the analyst does not know the right answer
Standard Operating Procedures
a written procedure that must be rigorously followed to ensure the quality of a chemical analysis
Control Chart
a visual representation of a confidence interval for a Gaussian distribution
Assessment
the process of (1) collecting data to show that analytical procedures are operating within specified limits and (2) verifying that final results meet use objectives
Method Validation
the process of proving that an analytical process is acceptable for its intended purpose
Specificity
the ability of an analytical method to distinguish the analyte from everything else that might be in the sample
Linearity
measures how well a calibration curve follows a straight line
Square of the Correlation Coefficient
measure of goodness of fit of data points to a straight line (R^2)
Accuracy
nearness of a measured value to the "true" value
Precision
the reproducibility of a result
Range
the concentration interval over which linearity, accuracy and precision are all acceptable
Detection Limit
the smallest quantity of analyte that is "significantly different" from the blank
Signal DL = Ydl = Yblank + 3s
DL (conc) = 3s/m
Quantitation Limit
the smallest amount of analyte that can be measured with reasonable accuracy
QL = 10s/m
Reporting Limit
the concentration below which regulatory rules say that a given analyte is reported as "not detected"
Robustness
the ability of an analytical method to be unaffected by small, deliberate changes in operating parameters
Standard Addition
known quantities of analyte are added to the unknown and the responses are recorded (keeps matrix effect constant)
Matrix Effect
a change in the analytical signal caused by anything in the sample other that the analyte
Internal Standards
a known amount of a compound, different from analyte, that is added to the unknown
Response Factor
(F) the relative response of a detector to analyte and internal standard