07/03/2017 (Agence Europe) – The definitive adoption of new rules on the marketing and monitoring of medical devices is getting closer. On Tuesday 7 March, the Council of the European Union approved the compromises reached on both regulations (medical devices and in vitro medical devices) following verification by lawyer-linguists. Readers may recall that these rules tighten up the monitoring of products considered dangerous and give the notifying bodies more powers (these are external...