How can we help you?

Clinical evidence is vital for medical products. Due to the growing complexity and innovation of the medical device industry a new legislation has to be met, the Medical Device Regulations (MDR). Previous Directives are no longer adequate since May 2017. The final transition deadline to comply with the MDR is May 2020.

It is therefore recommended to prepare now for the impacts of the new Regulation.

Please read the specific information for Industry-sponsored or Investigator-driven trials and find out how we can support.