NSF PROSYSTEM – Your Partner in Biomedical Engineering

NSF PROSYSTEM is a worldwide leading consulting and service company in biomedical engineering. The sustainability of our successful projects is the foundation of our longstanding customer relationships. Together with our customers we form the future of biomedical engineering by pointing out new chances as well as handling critical challenges. Our portfolio covers consulting, management of complex projects and interim management. It is our business to meet your special needs and to offer ideal solutions.

Learn all about the new Medical Device Regulation (EU) 2017/745 or the new In-vitro-Diagnostic Regulation 2017/746. Do you need support in implementing the new regulatory requirements? We are your compentent partner for implementing new requirements.  You develop software as part of a medical device or as a standalone medical device and want to secure conformity to existing standards? As a software development partner, NSF PROSYSTEM provides the required components.

NSF PROSYSTEM is working as an active member in standardization groups like for example: ISO 13485, ISO 14971, IEC 62366, IEC 60601 and IEC 62304/82304. Therefore we have influence on standardization politics and decisions. By co-creating standards we are able to strengthen your company’s position against the competition.

If there are any questions, or if you wish for a nonbinding quotation, please feel free to contact us.
Don’t miss the opportunity of attending one of our seminars or join us at this year’s symposium “Quality management for medical devices” as part of the series of lectures Hamburg Dialogue (“Hamburger Dialog”) in cooperation with Life Science Nord e.V..