Confirmed capabilities
Practical tools for the work between request and report.
Features are organized around the records, responsibilities, and controlled handoffs that keep a laboratory moving.
Request a Demo01 / Patient & request management
Begin with a stable patient record.
LIS-Live separates patient identity from visits and laboratory orders, preserving a clearer history as the patient returns.
- Patient identity with duplicate warning and audited override
- Visits, sources, physicians and referrers
- Laboratory orders with tests, panels, priority, and price snapshots
- Permission-aware global search for authorized users
02 / Specimens & testing
Follow the specimen, not a trail of disconnected notes.
Accessions connect ordered work to collection, receipt, processing, rejection, and recollection events.
- Accession and specimen records with Code 39 labels
- Collection, receipt, rejection, and recollection events
- Routine, Priority, and STAT ordering with TAT indicators
- Numeric, text, selection, and narrative result entry
- Demographic ranges, critical limits, and visible result flags when configured
03 / Results & reporting
Controlled review before release.
Submitted result values can move through independent verification and controlled release, with amendments preserved as new versions.
- Draft and submitted result states
- Independent verification option
- Permission-controlled release
- Append-only result versions and visibly amended reports
- Print-friendly A4 laboratory results
04 / Control & visibility
Give each responsibility a clearer workspace.
Canonical roles resolve to granular server-enforced permissions across protected routes and actions.
- Role dashboards and work queues
- Administrator, Front Desk, Cashier, Medical Technologist, Laboratory Supervisor, and Owner / Management roles
- Operational and financial reports with CSV exports
- Structured audit trail, including denied access and print or reprint events
- Secure login controls, session expiry, and password-change enforcement
Implementation note
Configuration must be validated with the laboratory.
Reference intervals, critical thresholds, specimen rules, approval and signature requirements, retention policies, and any interfaces must be configured and approved by the laboratory’s authorized owner or clinical lead before live use.
Discuss your requirements