Software As A Medical Device In Europe – New Regulatory Regime About To Enter Into Force – (Part 3 Of 6)
By EsqSocial Corporation 25/02/21
Having shed light on the relevance of the intended purpose of a medical device when determining whether software qualifies as medical devices software (“MDSW”) under the new EU Medical Device Regulation 2017/745 (“MDR”) in part 2 of our series of articles, in this part 3, we now turn to the issue of risk classification of such MDSW under the MDR......
By: MoFo Life Sciences