Aurevia (formerly Scandinavian CRO and QAdvis)

Aurevia offers consulting services within medtech regulatory compliance, as well as clinical research CRO services supporting pharmaceuticals, ATMPs, biologics, medical devices, and in vitro diagnostic (IVD) devices. The company was formed in 2025 when Scandinavian CRO, QAdvis, Artimed, Clinical Consulting, Kasve, and P.R.I.S.M.A. CRO merged to become Aurevia.

Our services for the healthcare, pharmaceutical, and medical technology sectors cover quality assurance, regulatory affairs, clinical studies, and training. Our proven expertise and knowledge benefit medical device and IVD manufacturers, pharmaceutical companies, and healthcare units around the world.