Service
Laboratory information system (LIS) verification
Your LIS must report exactly what your instruments and staff produced. MQS helps you verify that LIS-reported data matches the source for every element that reaches a patient report.
Who this is for
- Laboratory directors
- LIS administrators
- Laboratories installing or upgrading an LIS
Common challenges
- Untested interfaces after an upgrade
- Calculated results or reference ranges that differ from expectations
- No documented evidence of LIS checks
How MQS can support you
The exact scope is agreed with you after an initial consultation.
- Verification of patient ID and specimen data
- Results, units, and reference ranges
- LIS-calculated results
- Critical and amended result reporting
- Verification documentation
How the engagement works
- 1
Discovery
We learn about your organization, services, goals, and quality, regulatory, or expansion priorities.
- 2
Gap assessment
We review procedures, records, and practices against the standards that apply to you, and report findings plainly.
- 3
Action plan
We agree on priorities, responsibilities, and a realistic sequence of work.
- 4
Implementation support
We work with your team to implement quality systems, develop procedures, prepare applications where needed, and train staff.
- 5
Inspection support
We help you prepare for external inspections and can attend alongside your team.
- 6
Follow-up
We help you respond to citations and sustain improvements over time.
Frequently asked questions
Do you also verify EMR interfaces?
Yes. MQS provides EMR verification, including checks that results transfer correctly from the LIS into the medical record. We agree a system-specific scope with your team.
Talk to us about lis verification
Tell us about your quality, compliance, licensing, or growth priorities. We will recommend practical next steps.