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Fusions (Pan-Tumour ) [FFPE]

Product Code: 02-FUSION-27

From £796.00

Deadline to order: 28/02/2027

Fusion gene testing for fusions relevant to therapy (ALK, ROS1, RET, NTRK1, NTRK2, NTRK3, FGFR1, FGFR2, or FGFR3) for solid cancers (FFPE)

Target/Genes:

Fusion gene testing in FFPE tissue, for a range of clinically significant fusion variants, involving the following genes: ALK, ROS1, RET, NTRK1, NTRK2, NTRK3, FGFR1, FGFR2, or FGFR3.

Technology:

NGS, rtPCR

Language:

English, French, German, Italian, Spanish

Sample Type:

FFPE

Accredited:

Pending

Sample dispatch to your laboratory:

Sep-27

Test and Submit Results:

September - November 2027

Final Results and Certificate:

 May - June 2028

You can complete purchase on our secure partner site.

How it works

Register

  • Enrol before the closing date (28/02/2027)
  • EMQN ships EQA samples or digital cases

Test & submit results

  • Analyse samples in your routine workflow
  • Upload results via your website account (September - November 2027)

Review & get certified

  • EMQN assesses your data
  • Receive your individual results, EQA summary report & certificate of participation ( May - June 2028)

EQA Assessment

The scheme is designed to assess the entire diagnostic pipeline of a laboratory, including sample receipt and processing, analytical processing (genotyping), and reporting (biological and clinical interpretation of the test result) in the context of a clinical referral, as well as reporting clarity, content and clerical accuracy. 

Sample Details

 Three mock clinical cases with matching samples will be provided (1x 10um FFPE section). Samples are provided as cut sections (rolled scrolls / curls) only – we cannot provide slide mounted materials.

EQA Results

Participants will receive an individual report including educational advice and a scheme report which includes additional information from the cohort of participants including geographical spread, methodologies employed, common errors, learning points and scheme statistics allowing participants to benchmark their results. Each laboratory will also receive a single certificate listing all EQAs participated in with performance result for each year.

Participation Information

Participants are expected to test samples according to their routine strategy, to return a clinical report, and to complete the data collection form.  No restrictions on number of participants. Open to laboratories from ALL countries (note: some restrictions may apply due to sanctions, delivery network exceptions, restrictions on importation etc).

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