Continual improvement in quality
An asset to facilitate the laboratory accreditation process.
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. |
ISO 15189 accreditation process.
to save precious time.
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