Canopus Medical AB and Opera CRO

Canopus Medical AB and Opera CRO

Press releases Canopus Medical AB has contracted OPERA CRO to conduct its clinical trials in Europe Canopus Medical AB today announced that the company has entered an agreement for clinical services with the global contract research organization Opera CRO, for the...
Opera at Medica Trade Fair 2022

Opera at Medica Trade Fair 2022

Featured events Medica – World Forum for Medicine 2022 We are happy to announce that we will be joining the Medica Fair from the 14th of November till the 17th in Dusseldorf ??!The whole team is looking forward to seeing you, once again, in person after all of...
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...