Outcomes that are
measured, not claimed.

Our engagements are designed to produce measurable, sustained improvements. These are representative outcomes from completed engagements.

25–50%+
Throughput improvement
Across analytical, QC, and stability environments
Up to 87%
Cycle time reduction
Sample-to-result and batch release cycles
4–6×
Return on engagement investment
Measured over the 12 months following installation
<6 months
Typical time to measurable impact
From engagement start to sustained performance shift

Representative engagements and their outcomes.

60% Reduction in Analytical Cycle Time Without Capital Investment

A mid-size pharmaceutical manufacturer was missing batch release targets by an average of 4 days, creating downstream production delays and regulatory risk.

We installed a capacity model with workload leveling, redesigned the daily management rhythm, and introduced constraint-based scheduling to restore flow. Standard work was reframed around right-first-time controls. Visual management boards gave supervisors real-time line-of-sight into performance at the bench.

  • Analytical cycle time reduced from 11 days to 4.4 days
  • Right-first-time rate improved from 78% to 94%
  • Zero batch release failures in the 12 months following installation
  • Operating system fully internalised within 5 months

Turnaround Time Stabilised Across a 3-Site Pathology Network

A hospital network was experiencing high variability in pathology turnaround times, with outlier samples regularly exceeding clinical thresholds and generating escalations.

We mapped the demand and capacity model across all three sites, applied workload leveling to smooth volume spikes, and installed a tiered daily management system with visual management boards. Shift handover protocols were redesigned around standard work principles. A digital performance dashboard gave site managers real-time visibility into flow and constraint status.

  • Mean turnaround time reduced by 38%
  • Outlier rate (>2x target TAT) reduced by 71%
  • Shift handover incidents eliminated within 8 weeks
  • Dashboard adopted as standard management tool across all sites

Analytical Laboratory Aligned to Production Schedule for the First Time

A large food manufacturer's analytical laboratory was consistently unable to keep pace with production, creating hold-time risk on perishable product and significant waste.

We built a demand-capacity model linked to the production schedule, applied leveling to smooth sample arrival patterns, and redesigned prioritization to restore flow. Standard work was installed for sample prep and testing sequences. A daily management rhythm with visual management boards connected lab performance to production outcomes.

  • Product hold incidents reduced by 84%
  • Sample backlog eliminated within 6 weeks
  • Lab capacity model integrated into production planning process
  • Annual waste reduction estimated at €1.2M

30% Capacity Improvement Through Shift Structure Redesign

A high-volume clinical reference laboratory had reached an apparent capacity ceiling. Headcount had grown 22% over three years with no corresponding improvement in throughput. Unplanned overtime was chronic, waste was embedded in every shift, and leadership was preparing a capital case for facility expansion. The constraint was not space or headcount — it was how both were being used.

We built a demand-capacity model mapping specimen arrival patterns by hour, day, and day-of-week across a 12-week baseline. The model revealed that staffing peaks were misaligned with actual demand by an average of 2.5 hours per shift, and that significant analyst time was being consumed by non-value-adding activity — redundant checks, informal rework loops, and handover reconstruction. We redesigned shift start times, stagger patterns, and skill deployment across pre-analytical, analytical, and post-analytical phases. Waste was mapped and eliminated at the method level. Standard work for shift handover was installed to eliminate the information loss that was forcing incoming shifts to restart work already in progress.

  • Effective laboratory capacity increased by 30% without additional headcount
  • Unplanned overtime reduced by 40% within 10 weeks of implementation
  • Non-value-adding activity reduced by over 35% across all shifts
  • Capital expansion case withdrawn — existing footprint sufficient to absorb projected volume growth

Ready to discuss your environment?

Every engagement begins with a direct conversation about your operating environment, constraints, and objectives. No templates, no pre-packaged solutions.

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