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NSF Medical Devices Summit 2026

Join medical device manufacturers, regulatory specialists, quality leaders and technical experts in Hamburg, Germany on November 12 for a day of discussion focused on the challenges shaping today's MedTech industry.

NSF Medical Devices Summit 2026

Join medical device experts in Hamburg

Medical device organisations are navigating changing regulatory expectations, increasing software and AI oversight, evolving standards and growing pressure to expand into new markets.

The NSF Medical Devices Summit 2026 brings together industry experts and manufacturers to explore how organisations are responding to these challenges in practise.

Through expert presentations, industry perspectives and peer discussion, the programme examines topics including FDA inspections after QSIT, international market expansion, software and AI supplier management, U.S. submission readiness, platform technologies and the future IEC 60601/80601 standards landscape.

Full programme and speaker lineup now available

The full programme guide is now available, including the complete event agenda, session details and speaker biographies.

Hear perspectives from NSF alongside speakers from Olympus, B. Braun, Ypsomed, Karl Storz and Siemens Healthineers as they discuss FDA inspection expectations, international market opportunities, software and AI supplier management, U.S. submissions, product development and emerging standards.

Overview – NSF Medical Device Summit 2026

November 12, 2026 | Saalhaus, Hamburg, Germany

TopicSpeaker
OpeningMagdalena Müller, NSF
From Local Success to Global Potential: Recognising
International Market Opportunities
Katharina Stumborg, Olympus
& André von Malotki, NSF
From Market Opportunity to Market Reality: Lessons Learnt from Executing in ChinaKarim Djamshidi Gilani
Leveraging Platform Technologies for Product DevelopmentKarolina Snajdarova, Ypsomed
& Sandra Schaerer, Ypsomed
NSF Medical Device Research Study 2026: Global MedTech
Challenges, Industry Insights and Strategic Solutions
Sonja Redenius, NSF
The Future IEC 60601/80601 Series: Current Status, Structural Changes and OutlookRegina Geierhofer, IEC TC62
secretary / Siemens Healthineers
From Expectations to Implementation: A Structured Approach to Supplier Management for Software and AILukas Block, NSF
Preparing Established Products for U.S. Submission: How toprioritize gaps and minimise risksChristoph Erlen, B. Braun
& Eljar Amini-Nejad, NSF
FDA Foreign Inspections After QSIT: What Has Really
Changed?
Julian Thorns, NSF

A day built around real industry challenges

The 2026 programme combines regulatory expertise, manufacturer experience, and standards leadership across a range of topics affecting medical device organisations today.

Sessions explore how manufacturers are responding to changing FDA inspection expectations, evaluating opportunities beyond established markets, managing software and AI suppliers, preparing products for U.S. submission, and planning for future developments in the IEC 60601/80601standards series.

Industry speakers will also share lessons learnt from expanding into international markets and managing the realities of implementation once strategic decisions have been made.

The goal is not simply to present regulatory updates, but to provide context, experience and practical perspectives that help attendees better understand the challenges facing the industry.

Why attend

Delegates will gain practical insight into how MedTech organisations are responding to regulatory, technological, and operational changes across global markets. The summit provides a focused forum for understanding current expectations, learning from industry experience, and identifying practical approaches that support clearer planning, stronger decision-making, and more effective implementation.

Registration

Registration is now open for the NSF Medical Devices Summit 2026. 

Join medical device professionals in Hamburg on November 12 for a day of discussion, learning and networking focused on the challenges and opportunities shaping global MedTech.

How NSF Can Help You

Speak with NSF’s medical device experts about regulatory, quality and market access challenges across global markets.

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