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2.6.1.10.2 Criteria Used to Validate Data <br /> Integrity During Data Collection and <br /> Reporting <br /> 2.6.1.10.3 Methods Used to Identify and Treat <br /> Outliers <br /> 2.6.1.10.4 Reporting Scheme for Collection of <br /> Raw Data <br /> 2.6.1.10.5 Key Individuals In this Reporting <br /> Scheme <br /> 2.6.1.11 Internal Quality Control Checks (both Lab & <br /> Field) <br /> 2.6.1.11.1 Replicates <br /> 2.6.1.11.2 Spiked Samples <br /> 2.6.1.11.3 Split Samples <br /> 2.6.1.11.4 Control Charts <br /> 2.6.1.11.5 Blanks <br /> 2.6.1.11.6 Internal Standards <br /> 2.6.1.11.7 Zero and Span Gases <br /> 2.6.1.11.8 Quality Control Samples <br /> 2.6.1.11.9 Surrogate Samples <br /> 2.6.1.11.10 Calibration Standards & Devices <br /> 2.6.1.11.11 Reagent Checks <br /> 2.6.1.12 Performance and System Audits <br /> 2.6.1.12.1 Internal Audits <br /> 2.6.1.12.1.1 Description of Audits <br /> 2.6.1.12.1.2 Audited by <br /> 2.6.1.12.1.3 Frequency of Audits <br /> 2.6.1.12.1.4 Person to Receive Audit <br /> Reports <br /> 2.6.1.12.2 External Audits <br /> 2.6.1.12.2.1 Description of Audits <br /> 2.6.1.12.2.2 Audited by <br /> 2.6.1.12.2.3 Frequency of Audits <br /> 2.6.1.12.2.4 Person to Receive Audit <br /> Reports <br /> 2.6.1.13 Preventive Maintenance <br /> 2.6.1.13.1 Schedule of Maintenance to Minimize <br /> Downtime <br /> 2.6.1.13.2 Critical Spare Parts to Minimize <br /> Downtime <br /> 2.6.1.14 Routine Procedures Used to Assess: <br /> 2.6.1.14.1 Data Precision <br /> 2.6.1.14.2 Data Accuracy <br /> 2.6.1.15 Corrective Action <br /> A. Procedures Include the Following: <br /> 2.6.1.15.1 Limit for Data Acceptability beyond <br /> Which Corrective Action is Required <br /> 2.6.1.15.2 Re-evaluation of Analyst's Work & <br /> Instrumentation Checks <br /> 2.6.1.15.3 Corrective Action Initiator & <br /> Approver <br /> ec -A3-4- <br />