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
Turning your innovative ideas into ready-to-market products involves a highly complex development process. Our world-class engineers and scientists understand the unique requirements of life science and diagnostic applications, including molecular biology and automation systems development to fully cover your needs.
With a highly motivated and dedicated team and a state-of-the-art infrastructure, we have the resources you need to accelerate market introduction of your product.
Your project is in the right hands with us.