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PDF
Inter-Laboratory Comparisons & Proficiency Testing Workshop
Master external proficiency testing (PT) and inter-laboratory comparisons (ILC) : planning, execution, statistics, CAPA, and ISO-aligned reporting.
Home > Workshops > External Proficiency Testing and Inter-Laboratory Comparisons (ILC) Workshop
External Proficiency Testing and Inter-Laboratory Comparisons (ILC) Workshop
Inter-Laboratory Comparisons & Proficiency Testing Workshop
Workshop Index
Duration: 3 Days
Use the index to navigate the workshop sections and open quick reference modals for scope, audience, outcomes, delivery, policies, and FAQs.
Quick Summary
Overview & Outcomes
Agenda & Hands-on
Deliverables & FAQs
Quick View
Who Should Attend
Outcomes
Delivery
Policies
FAQs
Quick Summary
Quality Assurance
Hands-on Workshop
ISO Aligned
At-a-glance: PT / ILC design, statistics, and CAPA workflow
Understand external proficiency testing (PT) , inter-laboratory comparisons (ILC) , and where EQA fits your lab program.
PT
ILC
EQA
Build a practical plan for sample handling, chain-of-custody, timelines, and data integrity for ring trials.
Ring Trial
Chain Of Custody
Data Integrity
Work through scoring methods used in PT/ILC: z-score, robust mean/SD, En, and performance interpretation.
Z-Score
Robust Stats
En Number
Translate findings into corrective and preventive actions (CAPA) with root-cause analysis and evidence.
CAPA
Root Cause
Evidence
Align PT/ILC documentation to ISO 17043 concepts and lab accreditation expectations (where applicable) .
ISO 17043
Accreditation
Traceability
Produce a ready-to-use PT/ILC playbook: roles, checklists, acceptance criteria, and reporting templates.
Playbook
Checklists
Templates
Overview
Lab Quality Systems
Case Studies
Audit Ready
Scope, audience fit, and measurable learning outcomes
Clarify when to use PT vs ILC vs internal QC, and how each supports verification, monitoring, and continuous improvement.
Quality Control
Quality Assurance
Continuous Improvement
Define performance specifications: bias, precision, allowable error, and uncertainty-based acceptance limits.
Bias
Precision
Uncertainty
Map roles and responsibilities: technical lead, quality manager, analysts, data reviewer, and sign-off authority.
Roles
Governance
Review
Identify common failure modes: sample mix-ups, transcription errors, instrument drift, method changes, and contamination.
Pre-Analytical
Analytical
Post-Analytical
Learn how PT/ILC supports method validation, verification, and harmonization across sites or partner labs.
Validation
Verification
Harmonization
Apply outcome-driven reporting: interpret scores, document investigations, and communicate actions to stakeholders.
Interpretation
Investigation
Communication
Agenda
Statistics
Hands-on Labs
Practice First
3-day plan: design, execute, analyze, and close the loop
Day 1: PT/ILC fundamentals, program planning, provider selection, and building a yearly participation matrix.
Program Plan
Provider Review
Risk Based
Day 1 Hands-on: draft acceptance criteria and a PT/ILC SOP section for sample receipt, processing, and reporting.
SOP
Acceptance Criteria
Documentation
Day 2: statistical scoring and interpretation: assigned value, consensus value, robust algorithms, and uncertainty concepts.
Assigned Value
Consensus
Robust SD
Day 2 Hands-on: compute z-scores and En, create trend charts, and classify performance (satisfactory, warning, action) .
Z-Score
Trending
Performance Rules
Day 3: investigations and CAPA: root cause methods, containment, effectiveness checks, and management review inputs.
RCA
CAPA
Effectiveness
Day 3 Hands-on: write a complete PT/ILC closure report with evidence, deviations, actions, and audit-ready attachments.
Closure Report
Audit Trail
Attachments
Deliverables
Templates
Operational
Reusable
What you take back: documents, checklists, and FAQ guidance
PT/ILC annual plan template: participation matrix, risk-based prioritization, and review cadence.
Annual Plan
Risk Matrix
Cadence
Sample handling and reporting checklist: chain-of-custody, traceability, and data verification steps.
Traceability
Verification
Record Control
Scoring worksheet examples: z-score, robust mean/SD, En, and performance classification rules.
Z-Score
Robust Mean
En
Investigation and CAPA pack: RCA prompts, action tracking log, and effectiveness verification checklist.
CAPA
Action Log
Effectiveness Check
Audit-ready closure report template: deviations, evidence, impact assessment, and management review inputs.
Closure
Audit Ready
Management Review
FAQ guidance: participation frequency, method changes, result disputes, confidentiality, and multi-site harmonization.
Frequency
Method Change
Confidentiality
Quick View
Who Should Attend
Outcomes
Delivery
Policies
FAQs
Overview
PT, ILC, and EQA concepts, use-cases, and how they support lab quality systems.
Program planning, provider selection, and setting performance specifications and acceptance criteria.
Who should attend
Quality managers, technical leads, analysts, and lab supervisors running or supporting PT/ILC participation.
Teams preparing for audits or strengthening CAPA and documentation around external quality checks.
Learning outcomes
Interpret PT/ILC performance using z-scores, robust statistics, En, and trending.
Document investigations and implement CAPA with effectiveness checks and audit-ready evidence.
Agenda
Day 1: Fundamentals, program design, roles, and SOP-ready workflow.
Day 2: Scoring methods, interpretation, and performance classification.
Day 3: Investigations, CAPA, closure reporting, and management review inputs.
Hands-on / Demonstrations
Compute scores and classifications; build a trend view across rounds and sites.
Draft a PT/ILC closure report with attachments, evidence, and action tracking.
Deliverables
Annual plan template, sample handling checklist, scoring worksheets, CAPA pack, and closure report template.
FAQ
Participation frequency, method changes, dispute handling, confidentiality, and harmonization across labs.
Quick View
Close
Focus: external PT and ILC workflows from planning through closure reporting.
PT
ILC
EQA
Core skills: scoring (z-score, En), trend interpretation, investigations, and CAPA effectiveness.
Statistics
RCA
Audit Ready
Outputs: templates, checklists, and a repeatable playbook aligned to accreditation expectations.
Templates
Playbook
Governance
Use the other modals for audience fit, outcomes, delivery structure, policies, and FAQs.
Who Should Attend
Close
Quality managers and compliance teams building or improving an external quality program.
QMS
Audit
Governance
Technical leads and analysts responsible for PT/ILC execution, review, and sign-off.
Execution
Review
Sign-Off
Multi-site or partner labs aiming to harmonize methods, interpretation rules, and reporting.
Harmonization
Multi-Site
Collaboration
No prior advanced statistics required; concepts are taught with practical examples and worksheets.
Outcomes
Close
Plan PT/ILC participation with risk-based coverage, defined roles, and clear acceptance criteria.
Risk Based
Roles
Criteria
Interpret results using z-scores, En, robust statistics, and trending across rounds and sites.
Z-Score
En
Trending
Execute investigations and CAPA with evidence, effectiveness checks, and audit-ready documentation.
CAPA
Evidence
Audit Trail
You will leave with templates to operationalize these outcomes immediately.
Delivery
Close
Mix of guided instruction, worksheets, and scenario-based discussions from real PT/ILC lifecycles.
Case Studies
Worksheets
Lifecycle
Hands-on calculations and interpretation for scores and trends, with reusable rule sets.
Scoring
Rules
Reusable
Documentation practice: SOP updates, deviation notes, and closure reports designed for audits.
SOP
Deviation
Audit Ready
Delivery is structured for teams to adapt content directly into their QMS.
Policies
Close
Confidentiality: examples and shared case materials are discussed without exposing sensitive participant data.
Confidentiality
Privacy
Good Practice
Data integrity: emphasize traceability, reviewer checks, and controlled records for PT/ILC submissions.
Traceability
Record Control
Reviewer Checks
Change management: handle method changes and impact assessments between PT/ILC rounds.
Change Control
Impact
Consistency
Policies are operational guidelines for workshop practice and audit-ready documentation habits.
FAQs
Close
How often should we participate? Use risk, test volume, and clinical impact to set frequency and coverage.
Frequency
Risk
Coverage
What if a method changes mid-cycle? Document change control, re-baseline trends, and assess comparability.
Method Change
Comparability
Documentation
How do we handle disputes? Verify data, confirm traceability, and follow provider guidance with evidence.
Verification
Evidence
Provider Process
Can we compare across sites? Yes, with harmonized rules, shared acceptance criteria, and clear governance.
Harmonization
Criteria
Governance
FAQs focus on operational decisions labs face during PT/ILC participation.
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Workshop Enrollment
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Workshop
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