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Genomic EQA Directory

GenQA offer >120 genomics EQA covering thirteen different disciplines, encompassing the sample and patient journey. 

Free GenQA membership is required to purchase EQAs and enrol in individual competency assessments.

2026 EQA updates including 'early bird' EQA discounts.

 

GenQA supports truly global participation by accepting EQA submissions in English, French, German, Italian, Polish, Portuguese, and Spanish - breaking language barriers to ensure accessible, high-quality genomic assessment worldwide.

 

 2026 EQA price list (1st April 2026 - 31st March 2027)

 

2025 EQA price list (1st April 2025 - 31st March 2026)

 

GenQA LIVE calendar (includes EQA dates and other GenQA events)

Multidisciplinary team (MDT) working

Overview:

GenQA is the first genomic EQA provider to offer an EQA for the whole multidisciplinary team e.g. laboratory staff and clinicians.  Input from both scientific and clinical staff is critical to ensuring accurate interpretation of genomic testing results. These educational multi-stage scenarios are based on real cases requiring interpretation of clinical information and test results.

  • Genomic MDT rare disease EQA - To ensure the whole team is included, cases will be provided where either MDT discussion is required prior to issuing of the laboratory report, or where a laboratory report requires review or update following MDT discussion.
  • Genomic molecular tumour board (MTB) for lung cancer - An educational multi-stage case scenario based on a real clinical case requiring interpretation of test results, recording of MTB discussion and outcome of MTB. 

 

Summary information:

Assess your variant classification, clinical interpretation and reporting of a variety of results.

  • EQAs delivered in accordance with the international standard ISO 17043 for proficiency testing providers.
  • Cases based on real clinical scenarios.
  • 12 weeks to complete the case(s) and submit results.
  • Submitted results are assessed by an expert panel.
  • Each participant receives an Individual Centre Report (ICR) and EQA summary report detailing general findings, common errors and benchmarking against other participants worldwide.

 

Genomic molecular tumour board (MTB) for lung cancer (pilot) (MMTB)
An educational multi-stage case scenario based on a real clinical case requiring interpretation of test results, recording of MTB discussion and outcome of MTB. Pre and post MTB documentation are submitted along with a laboratory report.
Updated: 2026 EQA includes solid tumours and cfDNA for solid tumours
Genomic multidisciplinary team (MDT) working for rare disease (pilot) (MMDTR)
Multi-stage scenario requiring interpretation of test results pre and post MDT and submission of a laboratory report. This EQA is aimed at teams interpreting genomic data for rare and inherited diseases.