Critical result workflows should define thresholds, notification rules, escalation, documentation, and physician acknowledgement where policy requires it.
Quality and audit evidence
“Critical Result Workflow in LIS” should produce records the laboratory can demonstrate during internal or external review, not just a screen feature.
- Who changed what and when
- Link QC to instrument, user, and lot
- Clear procedure for critical and amended results
How Medrara supports this topic
Medrara is a cloud LIS that unifies orders, specimens, results, QC, inventory, and branches, with HL7/ASTM integration patterns and physician result delivery when configured and validated.
Related resources
cloud LIS for medical laboratories
This Medrara knowledge article is educational, not medical, legal, or regulatory advice. Validate implementation details against your local policies and contracts.
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