We offer clinical laboratories a wide range of internationally recognised products and services to help them maintain and improve analytical performance.
We provide QARA and clinical research services for the entire lifecycle of a medical device.
Our experienced team provides extensive clinical research services for pharma and biotech companies.
Our external quality assessment service program includes more than 250 quality assessment schemes.
We are an experienced, full-service CRO covering all phases of clinical development.
We help medical device companies with clinical research and regulatory compliance during the entire lifecycle of your products.
Our regulatory affairs services cover the entire lifecycle of medical and in vitro diagnostic devices.
Our experienced quality assurance professionals offer flexible services and tailored solutions.
See trainings related to clinical investigations.
This training series provides an efficient introduction to the regulatory essentials to turn regulatory compliance into a business advantage and to avoid the typical pitfalls of the health tech sector.
Trainings related to medical devices and regulation.
Good Clinical Practice training
Look into current topics in health sector and regulation with our experts.
The latest news from Aurevia. Keep track of what's happening!
Meet us at events.
Acronyms and terms in clinical research and regulation explained.
See our scientific posters presented at various congresses
Learn more about the companies we serve and the work we do.
Aurevia formed in 2025 when Artimed, Clinical Consulting, Kasve, Labquality, P.R.I.S.M.A., QAdvis & Scandinavian CRO merged as Aurevia.
We are happy to help you.
Our offices in different countries.
Interested in working with us? Check out our vacancies and apply!
Markus Vattulainen dataprotection@aurevia.com
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