Using the App
EQA Investigation Training
Premium tool. Open from /training-dashboard → EQA Investigation card (the dashboard uses the short label, without the "Training" suffix), or directly at /eqa-investigation-training.
UK NEQAS performance failures must be investigated and documented under ISO 15189:2022. This simulator drills the end-to-end process — from receiving the unsatisfactory report to closing the CAPA.
What it does
- Presents a simulated UK NEQAS performance report with a flagged result
- Asks you to apply the three-stage investigation: confirm the failure, identify root cause, plan corrective action
- Generates the NCAP / CAPA document based on your inputs
- Walks you through communication — who you tell internally, when you contact NEQAS, when you involve UKAS
- Simulates the re-verification sample cycle to close the loop
EQA failure types covered
- Single occurrence — one outlier in a generally-performing run
- Persistent poor performance — repeated outliers in the same scheme
- Systematic bias — consistent over/under-recovery suggesting calibration drift
- Comparator method discrepancy — your result is correct but disagrees with the peer group
- Scheme suspension — what to do when NEQAS suspends your participation
Root-cause analysis
The simulator uses the same RCA tools as the dedicated Root Cause Analysis Simulator:
- 5-whys — sequential cause chain
- Fishbone / Ishikawa — categorised by people, method, equipment, environment, materials, measurement
- Bowtie — combining cause analysis with consequence mitigation
You can pick any of the three and the simulator walks you through it.
Documentation produced
- NCAP (Non-Conformance and Action Plan) — short form for minor events
- CAPA report (Corrective and Preventive Action) — formal for repeat or significant events
- UKAS communication — if accreditation is affected
- Internal communication — section head, quality lead, line manager, lab director
Standards alignment
- ISO 15189:2022 clause 7.3.7 — EQA participation
- UK NEQAS Scheme Specific Operating Procedures (your scheme's current handbook)
- UKAS TPS 70 — pathology accreditation requirements
- MHRA for IVD-regulated devices that fail
- NHS England Pathology Quality Assurance framework
Bands and competency mapping
- Band 5 — recognise EQA failures, document, escalate
- Band 6 — lead the investigation, write the CAPA, communicate
- Band 7 — service-wide CAPA strategy, repeat-failure prevention, present at management review
Completed investigations are accepted as IBMS Specialist Portfolio (Quality Management section) evidence.
Pairs well with
- Root Cause Analysis Simulator — the underlying technique
- SOP Writing Simulator (article 43) — what often comes out of a CAPA
- UKAS Audit Training (article 44) — how external audit interacts with EQA
Common interview question themes
- "Walk me through how you would respond to a UK NEQAS unsatisfactory result"
- "What's the difference between a corrective and a preventive action?"
- "How do you close a CAPA — what evidence does UKAS expect?"
- "Tell me about a real EQA investigation you contributed to"