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AUREVIA

About us

Aurevia formed in January 2025 when Artimed, Clinical Consulting, Kasve, Labquality, and P.R.I.S.M.A. merged as Aurevia. 

Aurevia advances healthcare, pharmaceutical and medical technology development and quality with a future-focused approach, aligned with client needs.

We provide comprehensive CRO and regulatory affairs services, EQAS, auditing & certifications, and professional training for pharmaceutical, medical and IVD devices industries and healthcare organizations.

Our story: From separate histories to a shared legacy

Artimed, Clinical Consulting, Kasve, Labquality, and P.R.I.S.M.A. are now Aurevia.

Once we were individual pioneers in external quality assessments, regulatory consulting, and clinical research, now we stand united to form a worldwide powerhouse—not only a full-service contract research organization delivering rigorous science, proactive support, and solutions on a global scale but also a trusted EQA partner ensuring that clinical laboratory quality standards are met. With decades of combined experience, we bring a unique blend of expertise and innovation, setting new standards that go beyond what the market offers today.

Towards excellence in patient care

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

Pharmaceutical and Medical Device Contract Research Organization (CRO)

We provide comprehensive services and expertise for clinical research: Our offering covers medical and IVD devices from early development to post-market activities and pharmaceutical development from pre-clinical to phases I-IV. Our extensive  services cover the entire life cycle of a medical or in vitro diagnostic device from the early stages of product development to post-market surveillance. Our services are conducted in compliance with applicable regulations and industry standards.

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External quality assessment services (EQAS)

We offer clinically relevant external quality assessment schemes (EQAS) for medical laboratories and point-of-care testing sites to monitor and improve their performance and quality. Our external quality assessment (EQA) service program includes approximately 250 products, covering all specialities of laboratory medicine.

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Quality Assurance and Regulatory Affairs Services (QARA)

We offer global regulatory and quality services for medical devices and in vitro diagnostics. Our team of experienced experts provides medical device and IVD industries comprehensive quality assurance and regulatory affairs (QARA) services in compliance with applicable regulations such as EU MDR, EU IVDR & FDA.

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Audits & Certification

We offer audit and certification services for Finnish social and healthcare organizations to improve their management systems and quality e.g., with ISO 9001, ISO14001, SFS-EN 15224, and SHQS.

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Aurevia Academy

We offer professional training services on quality management, laboratory medicine and regulatory affairs including seminars, online courses, and tailored training programs.

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Aurevia leads the way in setting global quality standards that advance patient care and create lasting health impacts.

That's our vision.

We inspire excellence in our team every day to empower clients to achieve the highest clinical standards.

That’s our mission. 

AUREVIA'S CERTIFICATIONS AND ACCREDITATIONS

  • Aurevia’s management system is certified according to ISO 9001 (SBcert)
  • The main Labquality EQAS by Aurevia schemes are accredited according to ISO 17043 (FINAS, PT02, ISO 17043:2010)
  • The accreditation status of the EQA schemes is available in the scheme listing. The list of accredited schemes will be provided upon request.
  • Aurevia is an accredited certification body (FINAS, S023, SFS-EN ISO/IEC 17021-1:2015)