An asset to ISO 15189 accreditation
Our LIMS software includes multiple features that facilitate the accreditation procedure and simultaneously optimise laboratory efficiency.
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Who, what when and where?
Each and every action linked to patient data, test requests and specimens is saved to provide you with comprehensive traceability features.
- To preserve result confidentiality, the management of user rights allows you to control access rights based on both the origin of a request and the origin of the laboratory in which the user is situated.
- For authorised users, and as part of the unique patient record initiative cross-disciplinary visibility of results is a crucial factor during the clinical review phase and furthermore reduces the risk of result misinterpretation.
With the development of acquired antibiotic resistance nosocomial infections have become a major issue in public health.
- Alert mechanisms in the Microbiology module manage expert rules in real time in order to send an e-mail or SMS to a pre-defined list of recipients which in turn ensures that follow-up actions can be initiated.
- Threshold alert mechanisms send alerts when a certain number of cases reach predefined values.
- Dashboard with counters help you manage activity in real time
- Optimise sample management through effective work distribution
- Performance measurement and measure of time to results in real time using dedicated counters
- Targeted alert management by SMS or e-mail sent to a pre-defined list of recipients
- Record non-conformities in the LIMS
- Management and follow-up of corrective and preventative actions
- Follow-up indicators
Manage documents in accordance with accreditation requirements:
- Manage documents at every moment of their lifecycle (creation, authorisation, update and distribution)
- Automation of processes
- Document distribution which is subject to user rights