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January 22 - 24, 2018
United States

Robert Ezzell


Associate Director , Global Regulatory Affairs - Medical Devices
Sanofi


10:00 AM WHAT’S NEW IN THE REGULATORY?

•Join leading regulatory experts at this panel to evaluate Issues related to strategic implications of FDA device regulations
•Hear best practices for compliance with ISO 13485:2016
•Prepare yourself for the new EU Medical Device Regulations (EU MDR)
•Evaluate how MDUFA IV would impact the path to FDA approvals 


Check out the incredible speaker line-up to see who will be joining Robert.

Download The Latest Agenda