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' Section 8 <br /> . ONSITE Environmental Laboratories, Inc Revision 0 <br /> ' Quality Assurance Plan February 15, 1996 <br /> Page I of 1 <br /> ' 8.0 CALIBRATION <br /> Two types of calibration are discussed in this section <br /> > Operational calibration is routinely performed as part of instrument usage, such as the <br /> ' development of a standard curve for use with an atomic absorption spectrophotometer <br /> Each specific operational calibration procedure is described the SOP for the test being <br /> performed and is summarized in Appendix E, Table I <br /> ' > Periodic calibration is performed at prescribed intervals for equipment which can be <br /> calibrated at routine intervals, such as balances, ovens, or equipment This equipment <br /> has a distinct, single purpose urut and which is relatively stable in performance The <br /> ' specific calibration process for each piece of equipment is described in the Maintenance <br /> Log for that item and is summarized in Appendix E, Table 2 <br /> ' 8 1 Standard Preparation Logs <br /> Standard Prep logs are maintained that indicate how and when a calibration or QC <br /> standard was prepared, the intermediate concentrations, and by whom The logs also <br /> allow traceability back to the primary standard used An example of a standard <br /> preparation log is attached as Appendix F <br /> 82 Initial Setting of Retention Time Windows for GC <br /> ' If major changes in the instrument have occurred or a test procedure has not been <br /> previously performed at ONSITE, the laboratory is required to establish retention time <br /> acceptability windows by making at least three injections of all single component <br /> ' standard mixtures over the course of a 72 hour period Serial injections over less than <br /> a 72 hour period may result in retention time windows that are too tight <br /> ' The acceptance windows are established by calculating the standard deviation of the <br /> retention times from the three injections for each single component standard Plus and <br /> minus three times the standard deviation of the absolute retention time for each <br /> ' standard is used to define the retention time window However, the experience of the <br /> analyst, in consultation with the Laboratory Director or the Quality Assurance Program <br /> Advisor, may weigh heavily in the interpretation of chromatograms and the setting of <br /> ' windows In those cases where the standard deviation for a particular standard is zero, <br /> the laboratory substitutes the standard deviation of a close eluung, strrular compound to <br /> develop a valid retention time window <br /> 1 <br /> Word 6 0 loelsec$doc <br />