External Quality Assurance (EQA) programs assess laboratory analytical quality and reliability, enhance standardization efforts in clinical testing, and aid in corrective actions. EQA involves periodic assessments, comparison with target values, and participation in inter-laboratory comparisons, as mandated by ISO 15189. Choosing an EQA program requires careful consideration of factors such as sample commutability and participant numbers to ensure accurate lab performance.

1. EQAS
Dr Arun Sinha

2. Introduction
■ EQA can be called by different names
= external quality assurance
= external quality assessment
= proficiency testing scheme

3.  Definition
 process designed to objectively assess the quality
of results obtained by laboratories, by means of an
external agency

4. Objectives of EQA Programs
 Assess the laboratory’s analytical quality and reliability in
reported results
 Enhance worldwide standardization efforts in clinical testing
 Aid in identifying potential corrective actions and evaluate
their effectiveness
 Build confidence amongst the users towards lab performance

5.  To demonstrate a commitment for continuous
improvement and quality

6. Difference Between IQC &EQA
IQC/QC EQA/PT
Frequency Everyday/more
frequently
Periodically (once in a
month)
Target value Known Unknown
Result
availability
Immediately Later
Can assess Precision only Accuracy and
precision
Comparison Within lab With other labs

7. Iso 15189 Mandate For Eqas
 5.6.4 The laboratory shall participate in organized inter
laboratory comparisons, as external quality assessment
schemes, that encompass the extent and complexity of
examination procedures used by the laboratory.
 The laboratory management shall monitor the results of
external quality assessment and participate in the
implementation of corrective actions when control criteria
are not fulfilled.

9. The Process
Acceptable results verify that a lab is performing measurements correctly/ if
not corrective measures should be undertaken
EQA/ PT provider assigns or obtains a target value and determines if lab
results are in agreement with the target value
Results reported to the EQA/PT provider for evaluation
Each laboratory measures the EQA/ PT samples like patient samples
EQA/PT providers circulate a set of samples among a group of laboratories

10. Different EQA providers
Accredited under ISO 17043
Worldwide:
 RIQAS( Randox Quality Assessment Scheme),
 Biorad EQAS programme
 FCC EQAS
 CAP EQAS
In India:
 CMC (Vellore, TN)
 RML (Lucknow, UP)
 • Metropolis Healthcare Ltd. EQAS (Mumbai, MH)
 • Neu-QAP(Neuberg Anand Academy of Laboratory Medicine Pvt LTD Quality Assessment
Program).

11. Choosing An Eqas Programme
important questions to be answered
• Choosing the parameters which the lab wants to
put for external assessment. E.g

12.  How closely does the EQA/PT material match typical
patient samples in terms of Commutability*,
Homogeneity, Concentrations
 How is the target value established?
 What is the number of participants in the scheme and in a
particular method group?

13. Commutability

14. Sample Matrix

15. Schematic For Eqas In Laboratories

18. Parameter Settings

19. Result Reporting

20. Some key definitions
 Peer : other labs which are identical in method, instrument,
reagent combinations
for peer comparison there must be at least 9 reportable
results
 Method group: labs which use the same analyte and
method combinations but use other instruments and reagent
combinations

21.  Mode: all labs who perform the same analyte but
use different instrument, reagents and method
combinations

22. Interpretation Of EQAS Report

23. Interpretation Of EQAS Report

40. Take Home Message
 Eqas is an essential part of the total quality assurance
programme
 Even though it may appear cumbersome but it ensures
accuracy and precision of the reports generated by the labs
 Should be evaluated along with the IQC
 Documentation of the corrective action is must for quality
improvement

41. Thank you