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External Quality Assessment
Our external quality assessment (EQA) schemes are designed for medical laboratories and point-of-care testing sites to monitor and improve their performance. We provide objective and independent assessments, which support your existing quality system.
New schemes
We actively follow the development of laboratory medicine as we want to produce clinically relevant EQA schemes to serve clinical laboratories and point-of-care sites. We launch new pilot studies on a regular basis and aim to increase our EQA portfolio with 5-10 new EQA schemes every year.
IVDR compliance for in-house developed tests
The new In Vitro Diagnostic Medical Device Regulation (IVDR) has been applied in phases starting on 26 May 2022. The IVDR and the national law of each EU Member State also concerns in vitro diagnostics (IVDs) developed in-house by clinical laboratories. Such in-house developed tests include IVDs manufactured by the laboratory as well as CE marked IVDs that are modified by the laboratory.
Training services
We offer an even wider range of training services on quality management, patient safety and medical device regulation. Whether you're a quality expert, laboratory professional, development manager or radiology professional, we have the training that's right for you. Secure and maintain your skills!
Labquality Days
Labquality Days is one of the largest annual international congresses in Scandinavia focusing on quality in laboratory medicine and health technology. The inspiring atmosphere of the annual scientific congress gathers medical laboratory and health technology professionals together to exchange ideas and meet colleagues in Finland.
Contact us for more information
Juha Wahlstedt
EQA Sales Director
juha.wahlstedt@aurevia.com
+358 50 327 5338