Webinar: What US Companies Need to Know about Selling Medical Devices into the EU: Key differences between the EU & US Regulatory & Legal Environment

  • December 14, 2017
    12:00 PM - 1:30 PM

Please join the European American Chamber of Commerce and the United States Department of Commerce’s Commercial Services division for an expert presentation on the essentials for US companies to know about selling medical devices in the European Union. This program will cover:

* Changing regulatory framework: from EC Directives to the new Regulation;
* Classification of medical devices and borderline cases, software and apps;
* Main requirements for the marketing of medical devices in EU: the CE marking;
* Role of the notified bodies;
* Clinical evaluation and clinical investigations;
* Conditions for the advertising of medical devices and distance sales.

Detailed agenda to follow

Elisa Stefanini, Partner, Portolano Cavallo

web based program

Click here to Register