Table 1: Cross-references from ISO 17025 to ISO 15189 and ISO 15195
ISO 17025:2005 Clauses | ISO 17025:2005 Clause Titles | ISO 15189:2012 Clauses | ISO 15189:2012 Clause Titles | ISO 15195:2003 Clauses | ISO 15195:2003 Clause Titles |
---|---|---|---|---|---|
1 | Scope | 1 | Scope | 1 | Scope |
2 | Normative references | 2 | Normative reference | 2 | Normative references |
3 | Terms and definitions | 3 | Terms and definitions | 3 | Terms and definitions |
4 | Management requirements | 4 | Management requirements | 4 | Management system requirements |
4.1 | Organization | 4.1 | Organization and management responsibility | 4.1 | Organization and management |
4.1.5 | Organization | 4.1 | Organization and management responsibility | 4.3 | Personnel |
4.2 | Management system | 4.2 | Quality management system | 4.2 | Quality management system |
4.3 | Document control | 4.3 | Document control | 4.4 | Measurement documentation and records |
4.4 | Review of requests, tender and contracts | 4.4 | Service agreements | 4.5 | Contracting |
4.5 | Sub-contracting of tests and calibrations | 4.5 | Examination by referral laboratories | 4.5 | Contracting |
4.6 | Purchasing services and supplies | 4.6 | External services and supplies | 4.5 | Contracting |
4.7 | Service to the customer | 4.7 | Advisory services | ---- | ---- |
4.8 | Complaints | 4.8 | Resolution of complaints | ---- | ---- |
4.9 | Control of nonconforming testing and/or calibration work | 4.9 | Identification and control of nonconformities | ---- | ---- |
4.10 | Improvement | 4.12 | Continual improvement | ---- | ---- |
4.11 | Corrective action | 4.1 | Corrective action | ---- | ---- |
4.12 | Preventive action | 4.11 | Preventive action | ---- | ---- |
4.13 | Control of records | 4.13 | Control of records | ---- | ---- |
4.14 | Internal audits | 4.14 | Evaluation and audits | ---- | ---- |
4.15 | Management reviews | 4.15 | Management review | ---- | ---- |
5 | Technical requirements | 5 | Technical requirements | 5 | Technical requirements |
5.1 | General | ---- | ---- | 5.1 | Premises and environmental conditions |
5.2 | Personnel | 5.1 | Personnel | 4.3 | Personnel |
5.3 | Accommodation and environmental conditions | 5.2 | Accommodation and environmental conditions | 5.1 | Premises and environmental conditions |
5.4 | Test and calibration methods and method validation | 5.5 | Examination processes | 5.5 | Reference measurement procedures |
5.4.6 | Estimation of uncertainty of measurement | ---- | 5.6 | Metrological traceability ? Uncertainty of measurement | |
5.5 | Equipment | 5.3 | Laboratory equipment, reagents, and consumables | 5.3 | Equipment |
5.6 | Measurement of traceablity | 5.3.1.4 | Equipment calibration and metrological traceability | 5.6 | Metrological traceability ? Uncertainty of measurement |
5.6.1 | General | ---- | 5.3 | Equipment | |
5.6.2.1 | Specific requirements | ---- | 5.3 | Equipment | |
5.6.3 | Reference standards and reference materials | ---- | 5.4 | Reference materials | |
5.7 | Sampling | 5.4 | Pre-examination processes | ---- | ---- |
5.8 | Handling of test and calibration items | ---- | ---- | 5.2 | Handling of samples |
5.9 | Assuring the quality of test and calibration results | 5.6 | Ensuring the quality of examination results | 5.7 | Quality Assurance |
5.10 | Reporting the results | 5.7 | Post-examination process | 5.8 | Reporting results |
5.10 | Reporting the results | 5.8 | Reporting of results | ---- | ---- |
5.10 | Reporting the results | 5.9 | Release of results | ---- | ---- |
---- | ---- | 5.10 | Laboratory information management | ---- | ---- |