The MedTech Europe blog

Archives for scrutiny

It’s been a busy two weeks at the Parliament once again, with the release of both the draft report for the revision of the Medical Devices Directives (MDD) and that for the In Vitro Diagnostics Directives (IVDD) revision. Last Monday, EU Parliament Rapporteur Dagmar Roth-Behrendt published her draft report on the revision of the MDD.… » read more

Posted by MedTech Europe

If there is one thing that the medical devices industry agrees on it is that the new proposals for medical devices and IVD regulations are welcome and necessary evolution of regulation. What the industry also agrees on is that although it generally supports the new proposals, it is not certain at all that the proposed… » read more

Posted by MedTech Europe

With Eucomed’s annual MedTech Forum underway in Brussels this week, the European medtech trade association’s director of regulatory and technical affairs John Brennan gives the industry view on what is undoubtedly the hottest discussion topic among delegates at the forum: the European Commission’s proposed revision of the EU medical device directives. The European Commission’s proposal… » read more

Posted by MedTech Europe