MedQ Consultants B.V. will attend the RAPS EURO Convergence 2023 in Amsterdam
In exciting news, our VP Quality and Regulatory affairs will be attending the highly [...]
Clinical investigations under the MDR
The Regulation (EU) 2017/745 on medical devices (MDR) was created with the aim of [...]
MDR European Authorized Representative Services
MedQ Consultants B.V. will continue to provide EU Authorized Representative services under the [...]
Clinical trials during the CoVid-19 pandemic
It has been challenging to meet deadlines and milestones for the clinical trials [...]