The aim of the FAQ document is to answer some key questions on the new EU Medical Devices Regulation (MDR) 2017/745 and the anticipated impact on implementation activities and resources.
Please click here to read HealthLink’s MDR FAQ answers.
The aim of the FAQ document is to answer some key questions on the new EU Medical Devices Regulation (MDR) 2017/745 and the anticipated impact on implementation activities and resources.
Please click here to read HealthLink’s MDR FAQ answers.