Aurevia

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Aurevia was formed in January 2025 when Artimed, Clinical Consulting, Kasve, Labquality, and P.R.I.S.M.A. merged as Aurevia. Scandinavian CRO and QAdvis have also joined Aurevia. As Aurevians, we are the excellence makers: a team of experienced experts in healthcare and 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. We are a full-service, rapid-response Contract Research Organization (CRO) and external quality assessment services (EQAS) provider. Our quality services for the healthcare, pharmaceutical, and medical technology industries cover external quality assessments, quality assurance, regulatory affairs, clinical investigations and trials, audits and certifications, and training. Our expertise and knowledge benefit medical device and in vitro diagnostic manufacturers, pharmaceutical companies, healthcare units, and clinical laboratories. Currently, we serve over 8,000 customers in over 60 countries around the world. Our team comprises nearly 200 skilled professionals in offices in Finland, Sweden, Poland, and Germany
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Microbix & Aurevia Introduce Novel EQA Scheme - GlobeNewswire

Microbix & Aurevia Introduce Novel EQA Scheme GlobeNewswire

Aurevia Introduces Cross-Chain Solution to Enhance Blockchain Efficiency - CoinTrust

Aurevia Introduces Cross-Chain Solution to Enhance Blockchain Efficiency CoinTrust

Aurevia Announces Upcoming Next-Gen Blockchain Bridge for Seamless Cross-Chain Connectivity - openPR.com

Aurevia Announces Upcoming Next-Gen Blockchain Bridge for Seamless Cross-Chain Connectivity openPR.com

Aurevia Pine Review 2025: Legit or Not? - Canada Facts! - Republic World

Aurevia Pine Review 2025: Legit or Not? - Canada Facts! Republic World

FDA’s new CSA guidance: transforming software validation for production and quality systems - Life Science Sweden

FDA’s new CSA guidance: transforming software validation for production and quality systems Life Science Sweden

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