| EQA 2027 - Point-of-care testing (BD) |
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Expert Biologists - Program Coordinators:
Bernard POGGI, Marie LOPEZ and Laetitia SELMAN EQA performed since 2018
Number of analytical sites registered in 2026: 279, for Biochemistry / Haematology option (BDB) 22, for INR option (BDH) 20, for D-dimer option (BDDI) |
| Program organised by ProBioQual and placed under the aegis of the FAEEQ |
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1 – Program overview
This external quality assessment program allows you to check the accuracy of the results rendered by your point of care testing according to the standard ISO 15189. As the samples are ready for use, they can be analysed directly by healthcare staff as a real patient sample.
3 possible cumulative options (each option is sold separately):
For the 3 options, one registration allows access to 6 entries of results per analyte.
| Program limited to metropolitan France, Corsica excluded. |
2 – Assessment frequency
Biochemistry / Haematology (BDB) option:
INR Option (BDH):
D-dimer option (BDDI):
3 – List of analytes assessed
Biochemistry / Haematology option (BDB):
INR option (BDH):
D-dimer option (BDDI):
4 – Description of the control samples
Biochemistry / Haematology (BDB) option:
Fresh human control blood (1.2 mL samples, ready to use). Sampling carried out on the day of dispatch, delivered within 24 hours and to be assayed preferably on the day of receipt.
INR Option (BDH):
Liquid human control plasma (0.3 mL samples, ready to use)
D-dimer option (BDDI):
Liquid human control plasma (0.5 mL samples, ready to use)
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