Argos Multilingual
2 min. read
Understanding the Impact of the EU Medical Device Regulation (MDR) on IFUs
With the deadline for the implementation of the new Medical Device Regulation (2017/745) approaching, many life sciences companies, in particularly medical device manufacturers are in preparation mode. Executing a current state-analysis is the first step, but many companies are still unsure about what it is that’s changing and to what extent these changes will affect […]
