Our team consists of highly qualified experts who have years of experience in medical technology. We maintain a complete quality management system that meets the requirements of ISO 13485.
We listen to you! That gives us an understanding and a feeling of your company and your tasks. Based on the discusion, we develop strategies for the most cost-effective implementation of your project or medical product. In doing so, we focus on pragmatic and straight forward solutions that fit. We provide services in the areas of development, production and regulatory affairs - for large companies, for medium-sized businesses, for sience and start-ups.
Large medical technology companies trust our expertise. We provide services in the areas of regulatory affairs, quality management and documentation.
Small and medium-sized companies
We take the burden off you in development and production of medical technology components and in project implementation in the regulatory and normative areas.
When transferring research results into marketable medical products, many regulations have to be observed. Take advantage of our experience to reach your goal rapidly.
Start-ups in medical technology have ambitious goals. The borderline walk between technological implementation, compliance with regulations and realization within the defined time schedule is not always easy. We are happy to support you with pragmatic solutions that save your budget.
Solnovis was founded by Daniel Haberer.
Certificate ISO 13485
GTC for Work Service Supplies
GTC for the Supply of Goods and Services