Wash. Admin. Code § 173-50-061 - Required quality control practices
Laboratories must comply with the following quality control practices:
(1) Have a dedicated SOP
for each method listed on their current Washington scope of
accreditation.
(2) For parameters
where a multilevel calibration is necessary:
(a) A laboratory must not remove any
midpoints from a calibration curve with the exception of consecutive points at
either end of the curve. Exceptions can be made if a significant error's cause
can be clearly identified, the error is documented, and the calibration point
is excluded for all analytes contained in the calibration point.
(b) Each calibration point must have its
value recalculated against the calibration curve. Unless otherwise specified in
the method, each calibration point must have its percent error or relative
standard error meet the calibration verification acceptance limits from the
method; with the exception of calibration points at or below the LOQ, in which
case the limit is 50 - 150 percent error, or percent relative standard
error.
(3) For
parameters that require a limit of quantitation and the method does not specify
any requirements, laboratories must analyze a standard at their limit of
quantitation at least annually. This standard must be between 50 and 150
percent of the true value. This applies to the following instrumentation
technologies:
(a) Atomic absorption;
(b) Flow-injection analysis;
(c) Gas and liquid chromatography;
(d) Inductively coupled plasma;
(e) Ion chromatography;
(f) Spectrometry;
(g) Mass spectrometry;
(h) Total organic carbon analysis;
and
(i) Any other technology where
method detection limits are applicable.
(4) Matrix spikes are required as specified
by the method. Matrix spikes that do not meet their acceptance criteria must be
documented for regulated parameters under the federal Safe Drinking Water Act
and Clean Water Act. The lab must take corrective action if specified by the
method.
(5) Unless the method
specifies otherwise, laboratory control samples must include all analytes of
interest in the respective analysis. Matrix spikes should include all analytes
of interest in the respective analysis.
(6) For compliance monitoring samples, if a
laboratory control sample is outside of its acceptance criteria for a
parameter(s), the data for that parameter(s) should only be reported if the
laboratory can demonstrate:
(a) No source of
low bias of that parameter(s) is also present in the sample(s) and/or other
related quality control samples;
(b) Instrument calibration have met method
acceptance criteria; and
(c) The
reported samples do not have a detection for any high biased
parameter(s).
(7)
Documented resolution of spectral interferences is required for
ICP-OES.
Notes
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