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1 <br />~' <br />2.1.13 Analysis of Samples: At the time the samples are "logged in" at <br />the laboratory the laboratory's QA/QC program will be initiated. <br />All laboratory QC controls and methodology as defined in the <br />laboratory's Standard Operating Procedure (SOP) will be followed. <br />' A copy of the relevant sections of the analytical laboratory's SOP <br />document is attached as Appendix A. <br />2.1.14 Verify Analysis Performed as Re nested: Upon receipt of the laboratory <br />' analysis report the Project Manager will review the report relative <br />to the following criteria: <br />(1) that the analysis has been performed as requested; <br />' (2) that the correct analytical methodology was employed; <br />(3) that samples were analyzed within the holding times as <br />defined in Table 5; <br />' (4) that the in-house laboratory quality control sannples fall <br />' within prescribed limits and that a sufficient quantity <br />of QC samples were analyzed; <br />' (5) that the reporting format is correct; and <br />' (6) that the sample identities are reported correctly. <br />' 2.1.15 Quality Control Check of Analytical Results: If any items fall outside <br /> of the control limits of the quality control check the Project <br /> Manager will contact the laboratory to endea vor to resolve any <br /> discrepancies. If the problem encountered is a typographical error <br />the laboratory will issue a corrected report. Quality control <br />deficiencies affecting the validity of the analysis will be <br />' reported and discussed with the Project Manager to evaluate what <br />corrective measures should be taken. Anomalous valued will be <br />' -11- <br />I <br />