Robert Ezzell

Associate Director , Global Regulatory Affairs - Medical Devices
Sanofi

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

MAIN CONFERENCE DAY TWO

Wednesday, January 24th, 2018

•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