Toxicology LIS.
From screen to report.
KaiJun is a toxicology laboratory information system (LIS) in development for clinical laboratories. Explore how screening results, definitive testing, reports and daily quality records can fit into one considered workspace.
Discuss your laboratoryA laboratory information system for clinical toxicology
A clinical toxicology laboratory handles more than a result value. Staff need to connect the requested test to a specimen, understand the method used, review quality information and produce a report that reflects the work performed.
The KaiJun prototype brings together accessioning, screening and definitive result views, report layouts, reagent inventory and QA records. It uses synthetic examples so laboratories can evaluate the experience while production infrastructure and interfaces are developed.
- Order and specimen tracking in the demonstration workspace
- Separate screening and LC-MS/MS report views
- Instrument run dates and report release dates
- Daily maintenance, temperature and reagent lot records
Screening and definitive testing have different roles
The screening workspace presents immunoassay results as presumptive results. The definitive workflow has its own order and review context. In KaiJun’s example workflow, a physician can review a screening report before deciding whether to place a separate definitive test order.
Keeping those stages visible helps a laboratory discuss how its own ordering, review and release policies should be configured. A positive screening result in the demonstration does not automatically create a billable confirmation order.
Reports, inventory and laboratory quality management
The report collection includes selectable screening and definitive layouts. Users can explore the presentation of analyte results, cutoffs, method notes, instrument run dates and release information before choosing a laboratory report template.
The QA prototype also includes daily maintenance, temperature logs, SOP and policy records, and an audit workspace. Reagent inventory distinguishes screening analyzer lots from LC-MS stock and prepared reagents. These are demonstration features; retention, permissions, signatures and production audit protections require further implementation and validation.
Analyzer and EMR interfaces: the next workstream
Thermo Fisher Indiko Plus is the first planned screening analyzer connection. Beckman AU, Shimadzu and SCIEX workflows are also integration targets. SAVAS is the intended EMR integration workstream.
The current prototype uses simulated order and result exchange and synthetic LC-MS CSV imports. Live bidirectional analyzer interfaces and EMR delivery are not connected. Implementation depends on the exact instrument model, software version, vendor specifications and a documented interface validation.
Before you explore.
What does LIS stand for?
LIS means laboratory information system. In this context, it is software used to organize clinical laboratory orders, specimens, results and reports, with supporting laboratory quality records.
Can I try KaiJun with patient specimens now?
KaiJun is currently available as a synthetic-data prototype. Production safeguards, validated analyzer connections and laboratory approval are separate requirements before patient testing.
Start with your workflow.
Tell us about your instruments, reporting needs and the way your laboratory works.