Learn in just one day how to use large language models (LLMs) specifically in developing medical devices – from the initial idea to post-market surveillance.
This practical workshop with product expert Mario Klessascheck and regulatory and AI expert Prof. Dr. Christian Johner will teach you specific methods for drastically reducing your development time while remaining MDR-compliant.
Date | Title | Speaker | Location | Language |
Price
(plus VAT)
|
Free seats | Registration | |
---|---|---|---|---|---|---|---|---|
25.09.2025
|
Deutsch
|
980 €
|
|
Booked Out |
||||
14.10.2025
|
Deutsch
|
980 €
|
|
Booked Out |
||||
21.10.2025
|
Deutsch
|
1080 €
|
|
|||||
28.10.2025
|
Deutsch
|
980 €
|
|
You will learn how to use LLMs as brainstorming partners, development engineers, and reviewers for every development document, from requirements specifications to instructions for use. You will also understand the limitations of AI, enabling you to make informed decisions about where human expertise remains indispensable and where AI can provide optimal support.
100%
of the participants who gave feedback
recommend this workshop!
In hands-on exercises, you will use your familiar terminology to work on a specific medical device through all life cycle phases. You will leave the workshop with practical experience and be able to apply what you have learned directly to your devices – without any transfer effort.
The practical workshop shows you the path to becoming an “AI-first company” with a clear strategy map and practical areas for action. You will benefit from exchanging experiences with other companies, pass on your knowledge to colleagues, and become a valued digital transformation driver.
You will learn how to use large language models in accordance with MDR, IVDR, ISO 13485, and the AI Act, thereby meeting all regulatory requirements. With this knowledge, you can feel confident during your next audit and confidently refute objections from authorities and notified bodies – no more fear of non-conformities.
Prof. Dr. Christian Johner is the owner of the Johner Institute and an expert in the development and approval of medical devices that contain or are software. As an auditor, member of a standards committee, trainer for notified bodies, and author of several books and guidelines, he contributes to the further development of the regulatory landscape. His work includes guidelines developed for the WHO and notified bodies. He is also one of the most important contacts for the medical technology industry on AI. He has already created the AI Act Starter Kit and the AI Act E-Learning Course. Christian Johner has taught at several universities, including the University of Applied Sciences in Konstanz, the University of St. Gallen, the University of Würzburg, and Stanford University, where he focused primarily on software architecture, software quality assurance, and medical informatics.
Mario Klessascheck, electrical engineer (TU), has over 25 years of experience as an embedded developer for active medical devices. Since 2010, he has supported development teams as a safety consultant in understanding and applying standards such as IEC 60601-1 and safety and EMC tests. He is well respected in the industry as an author, lecturer, and trainer. His expertise also extends to medical systems engineering and functional safety.
We are also happy to offer you our seminars and workshops
in-house. Either online or at your premises, as required.
Please feel free to contact us.
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