Let's talk about your medtech project
Whether it’s custom development, industrialization, manufacturing, or a private label solution—we look forward to discussing your needs.
Markus Fritschi
MedTech Sales Manager
+41 52 647 50 96
How does a collaboration with Brütsch Technology start?
The first step is usually a non-binding initial meeting. We clarify requirements, objectives and framework conditions and define the next steps for a structured collaboration. A larger development project usually starts with a concept phase in which the requirements are specified, the feasibility is checked and the project is planned in detail.
At what stage of a project can you get involved?
You can join us at any stage – from the initial product idea and the further development of existing systems through to scaling and series production. We adapt our services flexibly to the project status.
Do you develop customized hardware and software?
Yes, we develop both hardware and software solutions, including electronics, embedded software, image processing and system integration. The goal is always an optimally coordinated overall solution.
How do you ensure quality and reliability?
Our processes are designed to meet high quality and safety requirements and we are ISO 9001 and ISO 13485 certified. This includes structured development processes, comprehensive tests, validated production processes and end-to-end quality management.
Can existing products be further developed or industrialized?
Yes, we also take on the optimization, industrialization or series transfer of existing products, for example to reduce costs, improve performance or adapt to regulatory requirements.
In what quantities do you produce?
We support both small batches and scalable series production. The production strategy is aligned with market expectations, cost structure and regulatory requirements at an early stage.
What standards and specifications are you guided by?
Our development processes are based on established standards and best practices such as IEC 60601, IEC 62304, IEC 62366, ISO 13485, ISO 14971, and the MDR and FDA requirements. These include structured design controls, end-to-end risk management, verification and validation activities, and comprehensive technical documentation throughout the entire product lifecycle.