Description
Download Quality Manual Format As per ISO/IEC 17025
- Ready to Use Manual
- Full Implementation Support
- Cover all necessary details required as per Standard ISO 17025:2017
- Unlimited Downloads
- Reference ISO 17025 Clause 5.3, 5.5
Table of Content
| ISO/IEC/17025:2017 Section | Contents |
| a. | Content of Quality Manual |
| b. | Amendment sheet |
| c. | Authorization |
| d. | Scope, Quality policy |
| e. | References |
| 3 | Abbreviations and Definitions |
| 4 | General requirements |
| 4.1 | Impartiality |
| 4.2 | Confidentiality |
| 5 | Structural requirement |
| 5.1 | Legal Identity |
| 5.2 | Management |
| 5.3 | Range of Lab. activities |
| 5.4 | Method of Organization |
| 5.5 | Duties & Responsibilities |
| 5.6 | Authority & Resources |
| 5.7 | Communication & Integrity of Management system |
| 6 | Resource requirement |
| 6.1 | General |
| 6.2 | Personnel |
| 6.3 | Facilities and environmental conditions |
| 6.4 | Equipment |
| 6.5 | Metrological traceability |
| 6.6 | Externally provided product and services |
| 7 | Process requirements |
| 7.1 | Review of request, tenders and contracts |
| 7.2 | Selection, verification and validation of
Methods |
| 7.3 | Sampling |
| 7.4 | Handling of test or calibration items |
| 7.5 | Technical records |
| 7.6 | Evaluation of measurement uncertainty |
| 7.7 | Ensuring the validity of results |
| 7.8 | Reporting of results |
| 7.9 | Complaints |
| 7.10 | Nonconforming work |
| 7.11 | Control of data and information system |
| 8 | Management system requirements |
| 8.1 | Options |
| 8.2 | Management system documentation |
| 8.3 | Control of management system documents |
| 8.4 | Control of records |
| 8.5 | Action to address risks and opportunities |
| 8.6 | Improvements |
| 8.7 | Corrective actions |
| 8.8 | Internal audits |
| 8.9 | Management reviews |
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