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| DOE-STD-1112-98
3.
identification of radionuclides for which the subject was analyzed and other
radionuclides detected
4.
type of measurement--lung, whole body, thyroid, etc.
5
quantification of the amount of radionuclides (whether positive, negative, or zero)
of each radionuclide measured in each part of the body counted
6.
estimates of counting uncertainty and the total propagated uncertainty (includes
counting and other random and/or systematic uncertainties) at the 1-sigma (1s )
confidence level
7.
value of the Lc and MDA, in the same units as results, and the expected Type I
and Type II errors
8.
the net count rate and standard error for measurements made for the purposes of
screening only, and not for a quantitative measurement
9.
the value of the customer-specified or service laboratory action level for prompt
notification (this may be documented elsewhere and need not appear in the report)
10.
the signature of the person responsible for the report or his/her designee.
b. Indirect Radiobioassay Information
1.
sample identification
2.
assigned number
3.
total volume or weight of sample submitted
4.
reference dates and times of sample collection and analysis
5.
identification of radionuclides for which the sample was analyzed and other
nuclides detected
6.
quantification of radionuclides using the appropriate blank values, whether
positive, negative, or zero
7.
estimates of counting uncertainty and the total propagated uncertainty (includes
counting, other random, and systematic uncertainties) at one sigma (1 s ) level
8.
identification of specific measurement procedures
9.
value of the Lc and MDA, in the same units as results, and the expected Type I
and Type II errors
10.
the value of the customer-specified or service laboratory action level for prompt
notification (this may be documented in the QA plan and need not appear in the
report)
11.
the signature of the person responsible for the report or his/her designee.
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