Lab Programmes

Registration

Please contact us for registration forms and price lists.

For centres in the UK, please contact neqas@coageqa.org.uk.

For centres outside of the UK please contact equalsbc@coageqa.org.uk.

Please scroll down for details of the laboratory programmes we run, and click on the links for further information on each programme, or click on the links to the left of this page. For point of care programmes, click here.

Participation in our EQA programmes requires agreement with the JWG

Please click on the links below for more information on our services

Laboratory Programme (Level 1: Screening Tests; Level 2 Assays)

This programme provides EQA for 30 different tests of haemostasis and thrombosis, including screening tests (e.g. PT, APTT, Thrombin time), anticoagulant control (e.g. INR, anti-Xa assays), factor assays and thrombophilia screening.

Molecular Genetics of Thrombophilia Programme

This programme provides EQA for centres testing for prothrombotic mutations FV Leiden and the Prothrombin gene mutation G20210A. EQA is also available for the C677T MTHFR gene mutation.

Genetics of Heritable Bleeding Disorders Programme

This programme provides EQA for genetics centres performing analysis of samples for heritable bleeding disorders, including Haemophilia A and B, von Willebrand's disease.

Homocysteine Programme        

Providing external quality assessment for assay of homocysteine.

DOAC (Direct Oral Anticoagulant) Assay Programme)

This programme provides EQA for laboratories performing assays for the following DOACs - Dabigatran, Rivaroxaban, Apixaban.

ADAMTS13 Assay Programme                         

This programme provides EQA for laboratories performing assays for ADAMTS13, for diagnosis and treatment monitoring of TTP.

Additional/Supplementary Exercises

We also carry out additional exercises, on an ad-hoc basis, for other assays and for educational purposes.

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