|04:00 PM - 05:00 PM JST|
|03:00 PM - 04:00 PM CST|
|08:00 AM - 09:00 AM BST|
This session will provide an overview of the EU regulatory framework, focusing on changes in regulation, including the new EU Medical Device Regulation, and current and future in vitro diagnostic (IVD) device regulation. We will also review the impact of Brexit on the life sciences industry, including the immediate impact of Brexit on medicinal product regulation.
CLE credit: CLE credit in CA, CT, FL, IL, NJ (via reciprocity), NY, PA, TX, and VA is currently pending approval.