The Swedish Life Science Industry Guide in Aurevia

Built on decades of experience and expertise

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 devices. With teams in the Nordics, Germany and Poland, we are highly skilled experts that support medical device and in vitro diagnostic (IVD) manufacturers, pharmaceutical companies, and academia throughout their product development. Our comprehensive services cover quality assurance & regulatory affairs (QARA), clinical studies, training, and more.

Aurevia was formed in 2025 when Scandinavian CRO, QAdvis, Artimed, P.R.I.S.M.A. CRO, Clinical Consulting, Kasve, Mectalent Medical Services, Lean Entries, and part of Labquality merged. In Sweden, our offices are located in Stockholm, Uppsala, Gothenburg, and Lund. Our international teams are headed by Ulrika Hammarström (Head of CRO) and Anna-Karin Alm (Head of QARA). 

"We value flexibility, clear communication, and close collaboration, which is truly appreciated by our customers."
- Anna-Karin Alm, Head of QARA & Ulrika Hammarström, Head of CRO