Our services at a glance
We offer comprehensive solutions to successfully bring your medical device or IVD to market. From user research for product definition, customized user interfaces & UX design to standards-compliant documentation and regulatory support, we are there for you every step of the way. Rely on our expertise to make your innovations safe and user-friendly.
User Research
Formative Evaluation
We test your product during development, derive improvements and prepare it for approval. Learn more…
Summative Evaluation / HF Validation
We support the approval process with standards-compliant summative evaluations / human factors validations. Learn more…
Design
UX & UI Design
We design outstanding UX & inspiring user interfaces with flawless usability. Learn more…
Product Design
We design your physical product to be inspiring and ready for production in the right quantities. Learn more…
IFU Design
Clear Instructions For Use are often important for safety & compliance. We design and test them for your product. Learn more…
Development
Front-end Development
We implement the UX & UI design of your product in code – regulatory compliant. Learn more…
Regulatory
Usability Documentation
We create your usability documentation, whether you are just starting out or need to improve existing documentation. Learn more…
Gap Analysis Technical Documentation
We identify and close gaps in your technical documentation and related processes. Learn more…
Post-Market Surveillance
We manage the PMS for you, including the development of related processes. Learn more…
Do you have a specific project you would like us to help you with?
Get to know us and our services in a no-obligation initial consultation with our experts.
Projects we are proud of
We want to meet you and your product!
