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Session 12: International Regulatory Updates and Insights
Session Chair(s)
Tamei Elliott, MS
Associate Director, Scientific Programs
DIA, United States
Receive the latest updates from international regulators and an industry representative on recent and future developments related to data standards, analytics, electronic submissions, and health authority IT programs. This session provides attendees the opportunity to ask regulators questions directly.
Please note: due to the high volume of questions, not all will be answered live at the forum
Speaker(s)
Speaker
Mick Foy
Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
Director of Delivery
Speaker
Hilmar Hamann, PhD
European Medicines Agency, Netherlands
Head of Information Management
Electric ERA (China eSubmission/eCTD): Revolution in Regulatory Affairs and Operations
Shenqi (Handsome) Ji
Pfizer, China
Regional Publishing Lead, Asia, Global Regulatory Operations
An Update on Health Products Standards and Innovation at HPFB
Nick Karitsiotis
Health Canada, Canada
Director of Business Innovation