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17.17 LMS Docs Flow Down Matrix

This document provides an overview of the procedures, work instructions, forms, and flow diagrams that make up an ISO 17025:2017 compliant Laboratory Management System (LMS). It includes the document title, procedure name, work instruction name, form number, flow diagram name, attachment number, and document name for each clause of the ISO 17025 standard. The document is structured with 5 levels that provide more detail on the management system documents from the overall LMS manual down to specific forms, instructions, and attachments.

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0% found this document useful (0 votes)
220 views1 page

17.17 LMS Docs Flow Down Matrix

This document provides an overview of the procedures, work instructions, forms, and flow diagrams that make up an ISO 17025:2017 compliant Laboratory Management System (LMS). It includes the document title, procedure name, work instruction name, form number, flow diagram name, attachment number, and document name for each clause of the ISO 17025 standard. The document is structured with 5 levels that provide more detail on the management system documents from the overall LMS manual down to specific forms, instructions, and attachments.

Uploaded by

faheemqc
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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ISO 17025:2017 LMS - Manual-Procedures-Forms-Matrix -P-xxx Numbers

QMS Level 1 - Topic Level 2 Procedure Level 3 - Work Work instruction Level 4 Form Flow Diagram Flow Diagram Name Attachment Attachment
Clause Procedure Name Instruction Name Form # Name # Name

All Laboratory Management System Manual - LMS-001

4&5 General and Structural requirements P-500 Management responsibility F-510-001 LMS-Process identification worksheet A-500-001 Quality policy
F-570-001 Comment and suggestion report A-560-001 Organization chart

6 Resource requirements P-610 Resource management F-610-001 Equipment problem report


F-610-002 Resource maintenance record
F-610-003 Environmental control log

6.2 Personnel P-620 Competence, awareness and training F-620-001 Training action plan
F-620-002 Group training record
F-620-003 Job description
F-620-004 Employee training summary

6.4 Equipment P-645 Control of monitoring and measuring equipment F-645-001 Equipment calibration list

6.6 Externally provided products and services P-660 Control of external providers F-660-001 Provider assessment report
F-660-002 List of acceptable sources
F-660-003 Provider corrective action request - PCAR
F-660-004 Purchase requisition
F-660-005 Purchase order
F-660-006 Business agreement - contract

7.1 Review of requests, tenders, and contracts P-710 Customer related processes F-710-001 Client assessment report
F-710-002 Order notification

7.2 Selection, verification and validation of methods P-720 Operational planning of methods F-720-001 Project planning worksheet
7.3 Sampling F-720-002 Method routing summary

7.4 Handling of test or calibration items P-740 Handling of test and calibration items F-740-001 Storage inspection report
F-740-002 External property control log
F-740-003 Identification tag / label
F-740-004 Laboratory activity log

7.5 Technical reports P-755 LMS-Monitoring, analysis, and evaluation F-755-001 Monitoring report
7.6 Evaluation of measurement uncertainty
7.7 ensuring the validity of results

7.8 Reporting of results P-780 Reporting of results F-780-001 Statement of delivery / invoice A-780-001 Test report - blank
A-780-002 Calibration report - blank
A-780-003 Report of sampling - blank
7.9 Complaint P-790 Complaints and nonconforming outputs F-790-001 Complaint response report
7.1 Nonconforming work F-790-002 Nonconformance report

8.2 Management system documentation P-820 Control of documented information WI-820-001 Document numbering system F-820-001 List of documented information
8.3 Control of management system documentation F-820-002 Records matrix
8.4 Control of records F-820-003 Master documentation lists
F-820-004 Quality records table
F-820-005 Document change request form
F-820-006 Document revision checklist
F-820-007 Software inventory spreadsheet
F-820-008 Revision status form

8.5 Actions to address risks and opportunities P-850 LMS-Risk management planning F-850-001 LMS-Risk management worksheet
F-850-002 LMS-Objectives planning record

8.6 Improvement P-860 Improvement F-860-001 Data analysis worksheet


F-860-002 Customer survey and analysis

8.7 Corrective actions P-870 Nonconformity and corrective action F-870-001 Corrective action request - CAR

8.8 Internal audits P-880 Internal audit F-880-001 Applicable procedure by work area
F-880-002 Internal audit checklist
F-880-003 Audit plan
F-880-004 Audit report

8.9 Management reviews P-890 Management review F-890-001 Management review agenda
F-890-002 Management review output report

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