Aurevia will attend the SPML's (Sociedade Portuguesa de Medicina Laboratorial) 17th scientific meeting on 3-5 April 2025 in Porto, Portugal. Aurevia's EQA Sales Director Juha Wahlstedt, and EQA coordinators from PNAEQ will be available for discussions at the exhibition of the meeting.
Please visit our booth to check our latest EQA programs and pilots!
Labquality EQAS by Aurevia - New schemes
We actively follow the development of laboratory medicine, and we want to produce clinically relevant EQA schemes to serve clinical laboratories and point-of-care sites. We launch new programs and pilot studies on a regular basis.
New schemes and 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
New EQA scheme for Pipette control
We have announced a new EQA scheme for controlling and monitoring single-channel piston-operated mechanical and electronic pipettes used in clinical laboratories.
This EQA scheme allows 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 obtained for each measurement (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
Registration and more information: 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 on a regular basis by participating in Aurevia’s EQA scheme.
7807 Preanalytics, pneumatic sample transport
Registration and more information: info@aurevia.com
See you in Porto!
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