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ISO17025 Quality Documents (Coming Soon)
Quality Manual
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Collection of policies that describe the laboratory’s method of implementing the quality management system requirements. Policies reference detailed quality procedures, as appropriate.
Quality System Orientation Procedure
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Document Control Procedure
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Review of Requests, Tenders, and Contracts Procedure
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Subcontracting Procedure
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1. Purpose
To define the system for evaluation and use of subcontract laboratories.
QP-005 I01 Purchasing Services and Supplies
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QP-006 I01 Action System
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QP-007 I01 Control of Records
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QP-008 I01 Internal Audits
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QP-009 I01 Management Review
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QP-010 I01 Training
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QP-011 I01 Accommodations and Environmental Conditions
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QP-012 I01 Test and Calibration Methods and Method Validation
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QP-013 I01 Equipment
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QP-014 I01 Sample Handling
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QP-015 I01 Quality Control
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QP-016 I01 Reporting the Results
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FRM-001 I01 Quality Records
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FRM-002 I01 Work Request Form
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FRM-003 I01 Customer Communication Form
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FRM-004 I01 Vendor Evaluation
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FRM-005 I01 Quality Critical Services and Supplies
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FRM-006 I01 Action Form
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FRM-007 I01 Effectiveness Review Summary
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FRM-008 I01 Incomplete Actions Summary
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FRM-009 I01 Complete Actions Summary
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FRM-010 I01 Quality Records
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FRM-011 I01 Internal Audit Form
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FRM-012 I01 Method Audit Form
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FRM-013 I01 Internal Audit Summary
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FRM-014 I01 Management Review Agenda
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FRM-015 I01 New Method Form
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FRM-016 I01 Housekeeping Form
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FRM-017 I01 Method Confirmation - Validation Form
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FRM-018 I01 Electronic Data Verification Form
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FRM-019 I01 Estimation of Measurement Uncertainty Form
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FRM-020 I01 New Method Checklist
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FRM-021 I01 New Equipment Form
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FRM-022 I01 Calibration Label
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FRM-023 I01 Out of Service Label
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FRM-024 I01 Equipment Maintenance Log
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FRM-025 I01 Sample Receipt Form
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FRM-026 I01 Sample Storage - Retention Log
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