About us
We advance healthcare, pharmaceutical and medical technology development with a future-focused approach, aligned with client needs.
Experts in clinical research and medtech regulatory compliance
Aurevia was formed in 2025 when Scandinavian CRO, Artimed, P.R.I.S.M.A. CRO, Clinical Consulting, QAdvis, Kasve, Mectalent Medical Services, and Lean Entries merged. Our services for the healthcare, pharmaceutical, and medical technology sectors cover clinical research, quality assurance, regulatory affairs, and professional training.
Our proven expertise and knowledge benefit medical device manufacturers, pharmaceutical and biotech companies, academia, and healthcare units around the world. In addition to our in-house capabilities, we leverage a robust network of trusted partners across Europe. When you collaborate with us, you gain access to the specialized knowledge and support that you need to succeed. In addition to our breadth and expertise, our relationship-focused approach makes all the difference and is truly valued by our clients.
Towards excellence in patient care
Our international team of experts has broad experience working in healthcare, health-tech standards and quality. Together, we advance healthcare, pharmaceutical and medical technology development with a future-focused approach, aligned with client needs. Driven by our commitment to care, we contribute quality to the industry and pave the way for safer, more effective patient care worldwide.
Aurevia leads the way in advancing patient care to create lasting health impacts.
That's our vision.
We inspire excellence in our team every day to empower clients to achieve the highest standards.
That’s our mission.
Aurevia Academy
We offer professional training services within quality management, regulatory affairs and clinical research including seminars, online courses, and tailored training programs.
