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Areas of expertise
- Medical devices
  Quality, regulatory and clinical research services for your entire medical device lifecycle.
- IVD medical devices
  Quality, regulatory and clinical research services supporting the development of your IVD device.
- Medical device software
  Expert consulting services to accelerate your medical device software development.
- Pharma & biotech
  Full-service CRO clinical trial services for pharma and biotech.
Services
- Pharmaceutical CRO services
  Expert CRO services for pharma & biotech, covering all phases of your clinical development.
- Medical device & IVD CRO services
  Full-service clinical research services for your medical device and IVD device.
- Medical device & IVD QARA services
  Quality assurance & regulatory affairs services covering the lifecycle of your medical device and IVD device.
News & events
- News & events
  Stay up to date with our latest news and events.
- Medtech Compliance Forum by Aurevia & RAPS
  Connect with industry peers & experts across the medtech community at our dedicated forum during Labquality Days, in collaboration with RAPS.
- Subscribe to our newsletter
  Stay updated on guideline and industry news, upcoming events, and expert tips relevant to your work.
- Customer success stories
  Examples of how we support life sciences companies in navigating regulatory, quality, and clinical research challenges.
Training & tools
- Courses
  Develop your team with our professional training services in quality assurance, regulatory affairs, and clinical research.
- Lean Entries
  Discover how our e-tools can help you turn complex regulatory requirements into actionable strategies.
- Glossary
  Browse our glossary of clinical research and regulatory terms.
- Log into Aurevia Academy
  Log into the Aurevia Academy portal to access your registered courses.
About us
- Our story
  Built on a legacy of excellence, we provide expert consulting services to the pharma, medtech and healthcare sectors.
- Careers
  Explore our career opportunities and join us in shaping the future of healthcare.
- Locations
  Browse our office locations across Europe.
- Contact us
  Contact our customer solutions team to get in touch with us.

Contact us

Speakers

The Medtech Compliance Forum by Aurevia & RAPS is a dedicated program within Labquality Days, bringing together regulatory and quality professionals, innovators, and medtech leaders to discuss the compliance topics shaping the future of the industry.

Catarina Carrao

Danielle Giroud

Erik Vollebregt

Ilkka Juuso

Janne West

Jari Martelin

Finnish Red Cross

Koen Cobbaert

Krishnadev Moothandassery Ramdevan

Lassi Rieppo

Mari Levula

Marika Karjalainen

Mihir Kelshiker

Molly Rogers

Reeta Levo

Reetta Hintsanen

Rina Wahlroos

Surash Surash

Contact us
Our customer solutions team is available from 9 AM to 5 PM (CEST; GMT +1).

+46 (0) 18 10 05 50
contact@aurevia.com

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Areas of expertise

Medical devices
IVD medical devices
Medical device software
Pharma & biotech

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