Practical Workshop "AI Power for Medical Device Development"
Faster to market with LLMs: From skeptic to accelerator in just one day
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.
Registration for the seminar Practical Workshop AI Power for Medical Device Development
If you have any further questions contact us directly .
PS: Would you like another appointment? Get in touch with us! Or consider an In-house seminar .
Minimize development time with LLMs – from idea to CE marking
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!
Immediately applicable – specifically for developing medical devices
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.
Become a sought-after AI expert in the team
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.
Develop with legal certainty – MDR and AI Act compliant with artificial intelligence
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.
You can find more information about the workshop and the schedule in the information sheet:
Further Information
AI models
- Types of generative AI models
- Tools, providers
- How they work “in a nutshell”
- Customization options: prompting, RAG, fine-tuning
- Adapting model parameters
- Optimizing prompts
- Generating product ideas
- Identifying customer requirements
- Identifying, checking, and supplementing product requirements
- Identification of hazards, risk analysis
- Design and review of a system architecture
- Software development (vibe coding)
- Deriving software, component, integration, and system tests
- Agents and agentic workflows
- MCP
- Company-owned AI
The path to an AI strategy map and an AI-first company
- Be able to assess which activities in the development process or product life cycle LLMs can help with and in what way
- Know the prerequisites (e.g., competencies) and limitations of AI
- Be able to write effective prompts
- Decide when to use prompts, system prompts, custom GPTs, RAG, and fine-tuning
- Assess your AI maturity level, identify gaps and areas for action, and name the characteristics of an AI-first company
- Know how to operate AI securely (IP protection)
- Be able to demonstrate to a notified body/authority that AI is being used in accordance with the law
These include, for example:
- Development Managers
- Developers
- Product Managers
- Managing Directors, Board Members, Division Managers, CEOs
Ideally, participants will already have experience working with technologies and be open to integrating new, innovative AI-based solutions into their everyday work.
An invoice will be sent to you within the next 48 hours, with a payment term of 14 days. If this payment term is not feasible for your company, please send a short e-mail to seminare@johner-institut.de to find a solution.
Three days before our online seminars and workshops, you will receive two e-mails: The first contains the final link to the workshop and the second contains the access data to a cloud folder in which you will find documents for preparation, exercises, and presentations.
If the seminar or workshop takes place in person, you will also receive the access link to your seminar documents three days before the date of the event. We will also provide documents in digital form for in-person events.
Our online/remote seminars and workshops are conducted via the video conferencing tool MS Teams. We recommend dialing in 20 minutes before the workshop begins so that any technical problems can be resolved in good time. If you have any questions or encounter any issues, our team is always available to help.
We also recommend that you arrive at the seminar room approximately 20 minutes before the start of the face-to-face events.
At the end of the workshop, you will receive a feedback link for evaluation. The following day, we will send you your certificate of attendance.
Get to know your trainers
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.
Are you familiar with our in-house seminars and workshops?
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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