Jan 27, 2014 | 8:00pm-8:00pm
Review of EU Medical Device Legislations Webinar
In 2008, the EU regulators launched a comprehensive review process of existing medical device legislations. The proposed texts covering medical devices and in vitro diagnostics are subject to a lot of discussion among different institutional groups and stakeholders. If adopted as currently proposed in 2014, the changes will significantly impact manufacturers. For example, the approval procedure for high risk devices has been radically changed and in vitro diagnostics will be classified differently in the future. If you are a U.S. exporter/manufacturer of medical or in vitro diagnostic devices and your target market is the European Union, you may want to sign up for this webinar.