Estimate the operational and financial impact of automation for your practice.
The financial cost is secondary. The real risk is the cognitive burden on physicians who must filter through hundreds of routine results daily, potentially missing subtle clinical patterns buried in the noise.
Cognitive clutter and fatigue-induced errors are the real cost -- not just the hours lost. When GPs process hundreds of routine results, the risk of missing a critical abnormality increases significantly.
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We partner with practices to reduce GP administrative time by approximately 30% using our Class I Medical Device automation. Think of it as a force multiplier -- removing the high-volume, low-complexity workload so your clinicians can focus on patients who need them.
That is equivalent to a partner getting home on time.
Rule 11(a) regulated. Our pathology automation system is certified as a Class I Medical Device under UKCA regulations.
Strict clinical risk management following DCB0129 standards, with documented hazard logs and safety cases.
Safety cases approved and maintained by a registered Clinical Safety Officer with ongoing clinical oversight.
Our system prioritises safety over sophistication. Every guardrail is adjustable per practice needs, ensuring clinical governance is maintained at every step.
Detects clinically significant changes between results
Age-based rules, PSA logic, and diabetes checks
Clinical keyword detection and flagging
Sample quality detection and error handling
GPs maintain full control at all times. The Merlin dashboard provides real-time visibility into what was auto-filed versus flagged, with a complete audit trail of every automation decision.
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