Aurevia’s international EQA team welcomes you to visit our exhibition booth A18 at BioMedica, which will be held from 19-20 March in Dublin. We have a joint exhibition booth with our partner, The Irish External Quality Assessment Scheme CLG (IEQAS) at the exhibition. IEQAS represents our Labquality EQAS by Aurevia external quality assessment service in Ireland. Aurevia and IEQAS proudly promote clinically relevant external quality assessment services for clinical laboratories and point-of-care testing sites.
EQA Sales Director Juha Wahlstedt and Key Account Manager Jukka Korhonen will be available to discuss during the exhibition hours. To book an appointment, please get in touch with juha.wahlstedt@aurevia.com.
EQA Programme 2025
Our EQA Programme 2025 includes over 300 clinically relevant products covering the main fields of laboratory medicine. There are also over 50 programs which are suitable for point-of-care testing. Download the product catalogue 2025 here.
New products 2025
- 5850 Brucella antibodies
- 5241 Bordetella pertussis/parapertussis, nucleic acid detection
- 5687 HBsAg and HCVAb POCT
- 5251 Interferon Gamma Release Assay (IGRA) for Mycobacterium tuberculosis - whole blood sample
- 5686 Norovirus, antigen detection
- 2755 Holotranscobalamin (HoloTC) and Methylmalonic Acid
For pricing and ordering information, please contact our local partner in your country or our customer service at info@aurevia.com.
Preanalytical EQA scheme for pneumatic sample transport
Does your pneumatic tube system (PTS) induce hemolysis? Is this preanalytical step included in your quality control process? Now you can easily monitor your PTS regularly by participating in our external quality assessment scheme.
7807 Preanalytics, pneumatic sample transport
Registration: info@aurevia.com
New EQA scheme for Pipette control
We are announcing a new EQA scheme for controlling and monitoring single-channel piston-operated mechanical and electronic pipettes used in clinical laboratories.
This EQA scheme offers a possibility for clinical laboratories to perform intermediate performance checks between pipette calibration intervals including interlaboratory comparison and individual performance assessment against a reference measurement value. The EQA samples provided in this scheme are noninfectious liquid samples. Participating laboratories are requested to perform multiple pipetting of a specific volume (100-1000 µL) and report the obtained mass weight for each measurement (a laboratory scale with 0.01 mg resolution is needed). Each laboratory may report results for up to 5 pipettes through the electronic platform LabScala. Result evaluations will be published in the final report distributed to the participants.
Note: This EQA scheme does not fulfil the accreditation requirements for pipette calibration, nor is it intended to replace standardized pipette calibration. Pipette calibration can be performed by ISO 17025-accredited calibration facilities or internally by the clinical laboratories when following the specified requirements. 8205 Pipette control
Vitamin D panel for method verification
As an exhibition promotion, we offer you a high-quality vitamin D panel with a 20% discount! Place an order through our customer service info@aurevia.com and mention the code EXHIBITION SALE to get the discount. The normal price of the panel is €1,750 + shipping costs and now €1,400 + shipping costs!
Contact us
Juha Wahlstedt
Jukka Korhonen
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