Medtech Compliance Forum by Aurevia & RAPS
Join us for a forum dedicated to medtech compliance, regulatory strategy, and clinical development, bringing together leading experts, industry professionals, and decision-makers.
What is the Medtech Compliance Forum?
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.
The forum continues the medtech program tracks that have been part of Labquality Days for the past seven years, now brought together under a dedicated international platform in collaboration with RAPS.
Organized by Aurevia in collaboration with RAPS, this initiative combines Aurevia’s regional expertise in quality, regulatory and clinical research with RAPS’s global network and international perspective. The forum brings together the Nordic and international medtech communities, creating a strong platform for thought leadership in medtech compliance. Read the full press release.
The Medtech Compliance Forum by Aurevia & RAPS will host scientific program tracks in health technology development and clinical evidence creation, combining global regulatory expertise, market insights, and practical real-world experience.
As part of Labquality Days, one of Northern Europe’s largest annual congresses in laboratory medicine and health technology, the forum benefits from an established, international platform. It provides valuable opportunities to learn, exchange experiences, and build connections that support innovation and compliance in medtech.
📍 Messukeskus Expo and Convention Centre, Helsinki, Finland
📅 SAVE THE DATE: 11–12 February 2027
The program for the Health Technology Development and Clinical Evidence Creation tracks will be announced in September. Registration is already open, and participants are encouraged to register early to secure their place and take advantage of the reduced early bird rates.
Who should attend?
The Medtech Compliance Forum is designed for:
- Quality & Regulatory professionals
- Medical device & IVD professionals and leadership
- Professionals working with clinical development and compliance
- Product and development managers
The forum is part of Labquality Days, an international event that celebrated its 50th anniversary during Labquality Days 2026. This leading Nordic event brings together professionals from laboratory medicine, medical & health technology, and clinical research to exchange ideas and build connections. It attracts a diverse mix of professionals, from hands-on specialists to decision-makers, creating a vibrant and collaborative network.
Labquality Days is an established international congress that:
- Attracts over 1200 participants
- Welcomes attendees from approximately 40 nationalities and 60 companies
Secure your spot
Register today and take advantage of early bird pricing.
Why attend?
- Learn from leading experts: Gain insights from respected voices in regulatory affairs, quality assurance, and clinical research across Europe and beyond.
- Stay ahead in a changing regulatory landscape: Explore key topics such as MDR, IVDR, clinical evidence, and regulatory strategy.
- Connect with the right audience: Meet professionals across healthcare, diagnostics, and the medical & health technology sectors.
- Turn compliance into opportunity: Understand how regulatory strategy can support business growth and market access.
Become an exhibitor
The Medtech Compliance Forum by Aurevia & RAPS is part of Labquality Days, one of Northern Europe's largest annual events focused on quality in laboratory medicine, diagnostics, medical & health technology, and clinical research.
As part of Labquality Days, the Medtech Compliance Forum offers exhibitors excellent opportunities to increase visibility, meet decision-makers, generate leads, and build valuable industry connections.
With more than 1200 participants from approximately 40 countries, the event provides a strong platform for both established companies and emerging innovators.
Previously, around 60 companies participated in the exhibition, creating a vibrant environment for networking, knowledge exchange, and business development.
The visitor profile includes specialists, employees, upper management, and decision-makers from across the healthcare, laboratory, diagnostics, and medical & health technology sectors, offering exhibitors valuable opportunities to connect with both existing and prospective customers.
Whether you are looking to showcase innovative products, strengthen your brand presence, build relationships, or engage with experts in quality, regulatory, and clinical evidence generation, the Medtech Compliance Forum provides a unique platform to reach a highly relevant audience.
Interested in becoming an exhibitor?
Information about exhibition packages, sponsorship opportunities, and participation options for the 2027 event will be published soon. Stay tuned for updates and discover how your organization can become part of this growing international forum.
Hosted together in partnership by:

