CE Marking according to the Medical Device Regulation

CE Marking according to the Medical Device Regulation

Insights CE Marking according to the Medical Device Regulation So what do you have to take into account to be allowed to place – or keep – medical devices on the European market under the new MDR? This blog post will briefly describe some of the important aspects, as...
MDR: What is considered sufficient clinical evidence?

MDR: What is considered sufficient clinical evidence?

Insights MDR: What is considered sufficient clinical evidence? Together with the introduction of Medical Device Regulation (MDR) 2017/745 clinical data become epicenter of many questions and even bigger need for medical device manufacturers. MDR expects from medical...