CLINICAL LABORATORY INFORMATION SYSTEM

A clearer LIS
for clinical
toxicology.

KaiJun is a laboratory information system in development for toxicology and pain management labs, connecting screening, LC-MS reporting and everyday quality work.

In development · Explore with synthetic data

KaiJun / Results & reports

RESULTS & REPORTSDemo workspace

Clarity, delivered.

Review complete*
KaiJun / LaboratoryCLINICAL TOXICOLOGY
01
SYNTHETIC EXAMPLE · NOT FOR CLINICAL USE
LABORATORY REPORT

Toxicology screening

SAMPLE
SPECIMENDEMO-1042Urine · Synthetic specimen
METHODImmunoassayPresumptive testing
Instrument runNov 07, 2026 · 09:42 PSTReport releasedNov 07, 2026 · 11:20 PST
AnalyteResultCutoff
AmphetaminesNegative1,000 ng/mL
BenzodiazepinesPresumptive positive200 ng/mL
BuprenorphineNegative5 ng/mL
MethadoneNegative300 ng/mL
INTERPRETATION

Screening results are presumptive. Definitive testing requires a separate authorized order in this example workflow.

Illustrative report · No clinical certification1 / 1
*Illustrative workflow state. Synthetic data only.
Every result has a story.Order. Run. Review. Release.
A CLOSER LOOK AT THE KAIJUN EXPERIENCE
FROM ORDER TO UNDERSTANDING
ScreeningLC-MSReportingQuality & audit
01 / THE PLATFORM

One considered workspace.
The whole laboratory day.

Developed around the real rhythm of clinical toxicology—from the first screen to the evidence behind every report.

Working synthetic workflow

A clear starting point.

Follow the specimen from accession to a reviewed presumptive result. Keep QC status and the physician’s next decision in view.

  • Order and specimen tracking
  • QC review before release
  • Separate definitive-test authorization
Screening workspaceDEMO
01
Order receivedSpecimen accessioned
02
Screen reviewedQC accepted in example
03
Physician decisionDefinitive order required
02 / THE FINAL IMPRESSION

Clinical detail.
Beautifully clear.

A report should feel as considered as the work behind it. Explore separate screening and definitive layouts, with instrument run dates and release dates clearly in view.

Configurable headers, report notes and layout defaults are available in the clinical prototype.

Illustrative report preview. Values and cutoffs are synthetic; this is not a validated clinical report.

KaiJun / LaboratoryCLINICAL TOXICOLOGY
01
SYNTHETIC EXAMPLE · NOT FOR CLINICAL USE
LABORATORY REPORT

Toxicology screening

SAMPLE
SPECIMENDEMO-1042Urine · Synthetic specimen
METHODImmunoassayPresumptive testing
Instrument runNov 07, 2026 · 09:42 PSTReport releasedNov 07, 2026 · 11:20 PST
AnalyteResultCutoff
AmphetaminesNegative1,000 ng/mL
BenzodiazepinesPresumptive positive200 ng/mL
BuprenorphineNegative5 ng/mL
MethadoneNegative300 ng/mL
INTERPRETATION

Screening results are presumptive. Definitive testing requires a separate authorized order in this example workflow.

Illustrative report · No clinical certification1 / 1
SIGNATURE / SCREENING SAMPLE
03 / A CONNECTED LAB

Built around your workflow.
Prepared for what comes next.

Connection work starts with the instrument, software version and vendor’s interface specification. Each interface is validated before clinical use.

WORKSTREAMPLANNED CONNECTIONCURRENT STATUS
01ScreeningIndiko Plus · Beckman AUSimulated order / result exchange
02Definitive testingShimadzu · SCIEXSynthetic CSV imports; live link pending
03Clinical coordinationSAVAS EMRUnconnected prototype handoff

Vendor names identify intended integration targets. Compatibility, licensing and vendor cooperation must be confirmed; no partnership or live connectivity is implied.

DESIGNED AROUND YOUR LABORATORY

Clinical toxicology LIS software.
A closer look at the workflow.

Explore how KaiJun’s laboratory information system prototype approaches drug screening, definitive testing and the clinical workflows that connect them.

04 / TRUST IS BUILT IN THE DETAILS

A deliberate path
to clinical use.

The product experience is taking shape. Production safeguards, vendor interfaces and laboratory validation are separate workstreams with explicit release gates.

Discuss your laboratory Product and business inquiries only. Please do not send patient information.
01Available to explore

Synthetic workflows, report layouts, QA records and interface simulations. The restricted clinical demo uses browser storage and is not approved for patient testing.

02Before real patient data

Production requires appropriate vendor agreements, individual accounts and MFA, server-enforced lab permissions, encrypted storage, protected audit records, tested recovery and a documented security assessment. These are planned requirements, not claims about this demo.

03Before clinical go-live

Validate instrument and EMR interfaces, QC and release controls, report accuracy, ordering and payer rules with the laboratory. Clinical release and claim submission remain distinct decisions.

04About this website

This is a product demonstration website, not a patient portal. We have not added advertising trackers, analytics or patient-data forms. The theme choice is saved in your browser. The hosting provider may process technical access logs under its own terms. Our contact page offers a direct email link and a business inquiry form. Form inquiries are processed by FormSubmit and emailed to Kokua Analytical Consultants. Please do not submit patient information.

LET’S BUILD A CLEARER LABORATORY DAY

Your workflow deserves
this level of thought.

Contact us

Discuss your laboratory, explore the platform or request a walkthrough.