Product Code: HBOC-25
From £445.00
Registration closed: 30/11/2024
Applicable to labs that undertake germline testing for this group of disorders
CNV, MLPA, NGS, Panel testing, Sanger sequencing
English, French, German, Italian, Spanish
DNA (in TE Buffer)
Yes
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.
Three mock clinical cases with matching samples will be provided for panel testing.
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.
*Sanctions, delivery network exceptions, restrictions on importation etc.
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