By end of 1998, the first European quality and safety requirements for in vitro diagnostic medical devices, the European Directive 98/79/EC (IVDD), stepped into effect. After almost 20 years in
Application automation and process adaptation − implementing the changes to physical workflow parameters and optimizing the way performance is checked − are essential for system development.
Thanks to our inhouse laboratories, we are able to test your application under real laboratory conditions. With a team of trained and highly experienced lab technicians and research associates, your application development is in the right hands with us.