V-Model of our development process

Quality Management

Qualified Design Process

Our development process is optimally suited for biomedical applications and conforms the related FDA and European norms. Based on a well-known V-Model it may be adapted according to specific customer requirements. Beginning with specific functional requirements we develop a precise description of the customer’s needs and propose a technical realisation. In order to optimize the design we  perform a continuous risk monitoring at every level of the design process. All our engineers and technicians fulfil the qualifications necessary for the development and manufacturing of biomedical devices and have at least three years experience in such branches as automotive, aerospace, military or medical device engineering.

„...open new Horizons“