Clinical research CRO services
We are a full-service contract research organization (CRO), offering services that support your clinical research. We support all phases of clinical development for pharmaceuticals, ATMPs/biologics, medical devices, in vitro diagnostic medical devices, and combination products.
Our international team consists of highly skilled experts with a proven track record and decades of experience working in clinical research. By partnering with us, you can be confident that we will provide expert support that enables you to succeed in your clinical studies.
Quality assurance and regulatory affairs services
We offer premium consulting services within medtech regulatory compliance. Our team of experienced experts provides medical device manufacturers with quality assurance (QA) and regulatory affairs (RA) services covering the entire lifecycle of medical devices and in vitro diagnostic medical devices (IVDs), from early development to post-market phases globally. With a proven track record of successful projects, we are ready to share our insights and support you throughout the development, market launch and post market surveillance of your medical device or IVDs.
Whether you are a startup or an established organization, our expertise spans across various medical devices and device classes. We collaborate closely with you and help you turn your vision into reality, mitigating risks and optimizing the timelines.
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Aurevia Academy
We offer professional training services within quality management, regulatory affairs and clinical research including seminars, online courses, and tailored training programs.
