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From November 16 to 19, 2026, we will be exhibiting at MEDICA in Düsseldorf. Visit us in Hall 17 | Booth 17B58 and talk to our experts about current challenges related to the MDR, IVDR, clinical evaluation, risk management, software, IVDs, biocompatibility, and AI in the regulated environment.
Whether you have specific project questions, need strategic guidance, or want to share experiences: Take advantage of MEDICA to have one-on-one technical discussions with our team.
Get in touch
Regulatory requirements for medical devices, IVDs, and health software are constantly evolving. At the same time, many manufacturers are under time pressure, must prioritize resources, and need to document regulatory decisions in a robust manner. At our booth, you can discuss specific questions, such as those related to:
Would you like to discuss your project situation in person or meet specific contacts?
Schedule an appointment in advance at our booth. This will allow us to arrange for the right experts to address your topic.
Possible topics of discussion:
![[Translate to English:] Andreas Thiel](/fileadmin/user_upload/Dozenten/Dr._Andreas_Thiel.jpg)
![[Translate to English:] Lesley Plön](/fileadmin/user_upload/Lesley_Ploen_1x1.jpg)
![[Translate to English:] Claudia Schmitt](/fileadmin/user_upload/Dozenten/Claudia_Schmitt_300x300.png)
![[Translate to English:] Margarita Rozhdestvenskaya](/fileadmin/user_upload/Margarita-Rozhdestvenskaya_1x1.jpg)
Margarita Rozhdestvenskaya will participate in the panel discussion at the MEDICA Tech Forum on the topic:
Compliance throughout the entire product lifecycle of a medical device.
Visitors who come to our booth via this landing page or our accompanying email will receive an exclusive reference book from the Johner Institute. Simply show the landing page and/or the trade show email on your smartphone to receive one of the following two books (German only, while stock lasts).
Enter our lottery right at our booth.
With our wheel of fortune, you have a chance to win:
Seminars, in-house training sessions, and workshops on regulatory and standards-related requirements.
Support with regulatory functions and project-related responsibilities.
Unterstützung entlang des gesamten Produktlebenszyklus – von Strategie bis Umsetzung.
Digital solutions and AI-driven approaches for regulatory processes and documentation.
Support for biosafety, biocompatibility, and other product-specific assessments.
MEDICA offers the opportunity to discuss regulatory issues directly with experienced professionals. Especially when dealing with complex issues, face-to-face discussions often help you better understand the requirements and plan your next steps more clearly.
If you’d like to discuss your current project, please feel free to visit us at MEDICA 2026 in Düsseldorf.
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![[Translate to English:] Florian Krafft](/fileadmin/_processed_/c/3/csm_Portrait_Florian_Krafft_300x300_Kopie_07f5c58d04.png)
![[Translate to English:] Pritu Detemple](/fileadmin/user_upload/Print_PrituFinalQuadrat.jpg)
![[Translate to English:] Katharina Keutgen](/fileadmin/user_upload/Katharina_Keutgen_300x300.png)
![[Translate to English:] Susanne Golombek](/fileadmin/user_upload/Susanne_Golombek_1x1.png)