On-Demand Webinar:
From Great Design to Great Code to Great Medical Devices: How to align IEC 62366-1 and IEC 62304
Webinar speaker: Dr. Benjamin Franz, Expert in software development, usability, and UI design for medical devices
Does this sound familiar?
Design and development are running at full speed in parallel. The user interface looks great, software development is progressing well, and the roadmap is ambitious. For a long time, everything seems to fit together perfectly.
But then the questions start piling up:
Why is this screen behaving differently than intended?
Which design decision was actually relevant to safety?
And why is it implemented this way now, even though it was conceived differently in the concept?
Suddenly, stress arises. Improvements are made, discussions take place, and explanations are given. Time is lost, risks increase, and by the time testing or audits come around, it becomes clear that design, usability, and software are not properly coordinated.
This is exactly where our webinar comes in: We show you how to use IEC 62366-1 and IEC 62304 not separately, but as a common framework – to align design, usability, and software from the outset and to safely pave the way from great design to robust code and an outstanding medical device.














Topics covered in the webinar:
In this webinar, you will gain a clearly structured overview of how design, usability, and software development interact effectively in medtech projects – and how you can use IEC 62366-1 and IEC 62304 together rather than separately:
- What constitutes “great design,” “great code,” and a truly great medical device – and why isolated excellence is not enough.
- Why design, usability, and software drift apart in practice – even in experienced teams – and what structural causes lie behind this.
- How IEC 62366-1 and IEC 62304 work as a joint process – with a concrete model that shows how usability engineering and the software lifecycle interlock.
The Details:
When is the webinar, "From Great Design to Great Code to Great Medical Devices: How to align IEC 62366-1 and IEC 62304," taking place?
This is a pre-recorded webinar. After registering, you will receive a link allowing you to view the webinar at any time within 90 days.
Can I ask questions?
Yes, you can ask questions at any time during the webinar. You will receive an answer via email afterwards.
How long will the webinar last?
The webinar will last approximately 70 minutes.
Who should attend the webinar?
This webinar is ideal for product managers, development managers, and software, usability, and regulatory experts in the medical device and IVD industry who want to coordinate design, usability engineering, and software development at an early stage – to avoid friction losses, reduce risks, and develop medical devices safely, efficiently, and in compliance with regulations.
What is the language of the webinar?
The webinar will be held in English.
Who is the speaker - Dr. Benjamin Franz?
Dr. Benjamin Franz is an expert in usability engineering and UI design for complex systems. For more than 15 years, he has been helping companies develop user-friendly and regulatory-compliant products. Some key points:
- Co-founder & Chief Growth & Innovation Officer of Custom Medical with locations in Germany and the USA
- Over 400 successfully completed medtech projects
- More than 10 design awards for user interface design
- TÜV Rheinland-certified usability expert for medical devices
- Author & Speaker
Watch “From Great Design to Great Code to Great Medical Devices: How to align IEC 62366-1 and IEC 62304” now for free
In this webinar, you will learn how to use IEC 62366-1 and IEC 62304 not as separate standards, but as a common process to effectively integrate design, usability engineering, and software development. You will receive a clear model of where breaks between design and code typically occur in real-world projects – and how to avoid them early on so that design intent, implementation, and regulatory evidence are consistently aligned. Based on over 400 successfully supported medtech and IVD projects.