Services
Our services for the healthcare, pharmaceutical, and medical technology sectors cover quality assurance, regulatory affairs, and clinical research services.
Expert consulting services you can trust
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 medical devices. Our services for the healthcare, pharmaceutical, and medical technology sectors cover quality assurance, regulatory affairs, clinical studies, training, and more. With teams in the Nordics, Germany and Poland, we are highly skilled experts that support medical device manufacturers, pharmaceutical companies, and academia throughout their product development.
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.
Our services
Clinical research CRO services
Quality assurance and regulatory affairs services
Quality assurance & regulatory affairs services covering the lifecycle of your medical device or in vitro diagnostic medical device.
Some of our clients