RAPS and the quality/regulatory consultancy Aurevia run this medtech compliance forum inside the broader Labquality Days congress, –, in Helsinki, Finland.
Date and format
- Date: 11–12 February 2027
- Format: in person, Messukeskus Expo and Convention Centre (Siipi Congress Wing), Helsinki, Finland
- Organizers: RAPS (Regulatory Affairs Professionals Society) and Aurevia, part of the Labquality Days congress
- Registration: early-bird €530 (1-day) / €570 (2-day), excl. VAT, per Aurevia's own programme page at verification
What it covers
Aurevia's own announcement of its new partnership with RAPS describes the forum's programme as covering health technology development, clinical and performance evidence, and IVDs — the kind of MDR and IVDR compliance questions device and diagnostics teams work through as part of a Notified Body submission or post-market surveillance plan.
Who should attend
Regulatory affairs and quality professionals at medical device and IVD companies working EU MDR or IVDR compliance, clinical evidence generation, or Notified Body engagement — and anyone attending the wider Labquality Days congress who wants the medtech-specific track.
Need a broader EU regulatory grounding first? TOPRA's Overview of EU and UK Regulatory Affairs course runs the same season, and the EMA SME Info Day covers the development-to-authorisation path from the regulator's own side. The full events directory lists everything we have verified.
Frequently asked questions
When and where is the Medtech Compliance Forum by Aurevia & RAPS?
11–12 February 2027, in Helsinki, Finland, at the Messukeskus Expo and Convention Centre's Siipi Congress Wing, as part of the Labquality Days congress, per RAPS's and Aurevia's own event pages.
Who organizes it?
RAPS (the Regulatory Affairs Professionals Society) and Aurevia, a quality and regulatory consultancy, co-run the forum within the broader Labquality Days congress.
What does the forum cover?
Aurevia's own announcement describes the programme as covering health technology development, clinical and performance evidence, and IVDs — medical device and IVD regulatory topics such as MDR and IVDR compliance.
What does it cost to attend?
Aurevia's own programme page listed an early-bird rate of €530 (1-day pass) or €570 (2-day pass), excluding VAT, at our last verification; confirm current pricing with the organizers before registering.
Sources & further reading
- RAPS. Labquality Days — event listing, 11-12 February 2027. raps.org
- Aurevia. Medtech Compliance Forum by Aurevia & RAPS - part of Labquality Days: 11-12 February 2027 — partnership announcement. aurevia.com
- Labquality Days. Scientific Programme — venue and congress details, 2027. labqualitydays.com
Event details are published by the organizers and can change. This listing was verified via WebSearch cross-corroboration of RAPS's, Aurevia's and Labquality Days's own pages rather than a direct fetch, because this session's network egress could not reach any of those hosts directly — confirm date, venue and registration with the organizers before making plans. Last verified 20 October 2026.
