Head of Global Software Standards
MAIN CONFERENCE DAY TWO
Wednesday, January 24th, 2018
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