Expert consulting services in clinical research and medtech regulatory compliance

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) medical devices. The company was formed in 2025 when Scandinavian CRO, Artimed, P.R.I.S.M.A. CRO, Clinical Consulting, QAdvis, Kasve, Mectalent Medical Services, Lean Entries, and part of Labquality merged to become Aurevia.

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