Towards excellence in patient care
We advance healthcare, pharmaceutical and medical technology development with a future-focused approach, aligned with client needs.
Our customer-centric approach means that our client’s needs guide our focus to create impactful results.
We prioritize transparency, dependability, and delivering high-quality results.
We deliver agile, tailored solutions through deep expertise and a commitment to excellence.
Expertise 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) devices.
With decades of combined experience, we support our clients with deep expertise to help them achieve their milestones and accelerate their product development.
Our services
Clinical research CRO services
Full-service CRO supporting pharma and medical device companies, as well as academia, to design and conduct their clinical research.
Quality assurance and regulatory affairs services
Quality assurance & regulatory affairs services covering the entire lifecycle of medical devices and in vitro diagnostic medical devices.
Some of our clients
Aurevia Academy
We offer professional training services within quality assurance, regulatory affairs, and clinical research including seminars, online courses, and tailored training programs.