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| DOE-STD-1121-98
C
listing of arrangements between the internal dosimetry program and the bioassay
measurements laboratory, including
-needed turnaround times
-MDAs for special and routine samples
-priorities for classification of samples (e.g., routine, special, emergency)
3.1.2 Bioassay Program Design
C
physical and chemical characteristics of radioactive materials encountered in the
workplace
C
establishment of the type and frequency of measurements to be used (RadCon
Standard 522.3)
C
derivation of decision levels
C
default trigger levels
C
preliminary actions to be taken for exposures to the different radionuclides present
at a facility following suspected or confirmed intakes at various levels
C
tailoring of investigations to a specific individual worker or exposure circumstances
C
documentation of the derivation of DILs
C
established DILs for each bioassay method applied for the analysis of all
radionuclides to which workers are likely to be exposed
C
if it is known or is likely that an individual has or could have intakes during the year
from different sources that could result in doses above the IL, methods to use to
derive an appropriately smaller DILs
C
methods of bioassay measurement and the rationale or justification for each
C
the MDAs for the bioassays
C
justification for the bioassay monitoring frequencies, including an evaluation of the
largest internal dose (i.e., minimum detectable dose) from an intake (acute or
chronic) that could go undetected with the chosen frequency
C
documentation and justification of a planned supplementary approach for intake or
dose assessment in case of technology shortfall
C
the rationale for the formal action procedures following a bioassay result
unexpectedly above the DL.
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