Continual improvement in quality
An asset to facilitate the laboratory accreditation process.
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This module enables you to manage non-conformities detected within your laboratory as well as external claims. From non-conformities identification to closing, including action plans implementation and assessment, it contributes to meet ISO 15189 requirements. |
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ISO 15189 accreditation process.
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to save precious time.
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This module helps you in complying with the ISO 15189 requirements and in getting the whole laboratory staff involved in your plan to constantly enhance Quality.
- Record non-conformities detected in the laboratory from wherever you are working
- Record complaints and enhance the quality of your laboratory service
- Manage and follow corrective or preventive action plans
- Measure your laboratory efficiency by using quality indicators
Save time in your day-to-day work by managing non-conformities in the most efficient way.
- User interface fully integrated into the LIS
- Easy and quick access
- Easy and quick access
- Tools that record non-conformities
- Efficient data entry tool to gathers significant information for non-conformities
- Efficient data entry tool to gathers significant information for non-conformities
- Contextual information recovery
- From wherever the non-conformity is recorded (request number, process, etc …)
- From wherever the non-conformity is recorded (request number, process, etc …)
This module allows you to closely track non-conformities detected in the laboratory:
- Track non-conformities related to a request by using specific indicators in the request
- Display non-conformities in result reports or request files
- Follow the cycle of nonconformities and measure the actions taken
- Close actions and related non-conformities when you think it is appropriate to do so
- Useful statistics to track non-conformities and monitor your laboratory
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