MDI | CERTIFICATION | EVENTS

Consultation Day Medical Devices 2026

We are pleased to continue the Consultation Day Medical Devices this year, following the success of our last event.

A forum for expert exchange in medical device regulation

In a regulatory environment that continues to evolve, the exchange of information and experience remains an important basis for informed decision-making. Professionals working in medical device sector are required to stay up to date with regulatory developments while maintaining a structured approach to compliance and quality.

We think that direct dialogue is an essential element of effective knowledge sharing. For this reason, we would like to invite you to the Consultation Day Medical Devices 2026 at the TÜV NORD site in Essen.

The event offers consultants the possibility to connect and discuss all the relevant topics. Participants will also receive insights into medical device certification and conformity assessment from the perspective of TÜV NORD as a Notified Body.

Participation is free of charge, but places are limited. Therefore, we recommend registering early if you would like to join the event and exchange with other professionals.

Register now free of charge

Important information about the event

Date & Time: October 15, 2026 | 10:00 AM – 5:30 PM
Location: TÜV NORD Site in Essen
Evening event: Networking with food and refreshments in a relaxed setting after 5:30 PM.
Participation: Free of charge (limited number of participants)

Please note: This event will be held entirely in German.
Food and drinks will be provided during the event.

What you can expect from this event

The latest developments from the Notified Body
Gain insight into the latest developments at TÜV NORD CERT. Our experts will keep you informed about regulatory changes, internal processes, and current challenges that may be relevant to your consulting work.

MDR 2.0: Current developments

The planned changes under MDR 2.0 are the subject of intense discussion. At our event, we will discuss these latest developments and assess their potential implications for manufacturers and consultants.

AI and medical devices

Artificial intelligence is becoming an increasingly important driver of innovation in medical technology. Learn about the regulatory requirements that manufacturers will face, as well as the developments that will shape the industry in the coming years.

MDSAP, clinical studies, consultation procedures, and other specialized topics

The event will feature expert presentations on current topics, including MDSAP, clinical studies, consultation procedures, and other regulatory issues. Our experts will share their experiences, offer valuable insights, and discuss common pitfalls.

The World Café format was used at the TÜV NORD event.

TÜV NORD World Café: Current topics and developments in the medical device industry

As part of the event, we will host an interactive World Café format. In moderated small-group sessions, participants will discuss current topics and developments in the medical device industry.

This interactive format offers a unique opportunity to exchange perspectives with fellow experts, discuss practical implications, and receive first-hand insights directly from representatives of the Notified Body. The focus is on open dialogue and shared expertise.

Register now free of charge

Date and location of the event

Date & Time: October 15, 2026 | 10:00 AM – 5:30 PM

Location: TÜV NORD Site in Essen
Am TÜV 1
45307 Essen, Germany

Highlights from our last event

Watch the video to see highlights from our most recent Consultation Day Medical Devices!

Join us for our free Consultation Day Medical Devices on October 15, 2026, in Essen

Register now for free

Additional downloadable resources

Discover more information about our services

Booklet

MDR-Booklet including M5

This booklet provides a comprehensive overview of the EU Medical Device Regulation (MDR), including the M5 amendment.

Request the MDR booklet now

Webinar recordings

IVDR webinar series

Request the recordings of the IVDR webinar today and discover directly from our expert, Thomas Fritzsch, how you can confidently implement the IVDR and how TÜV NORD, as a Notified Body, can support you with conformity assessment.

Request webinar recordings