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IMPACT OF THE REGULATIONS IN PRACTICE ACROSS REGIONS
Session Chair(s)
Michelle O'Connor, DrSc
Director Regulatory Consulting,
ICON Clinical Research, Ireland
Learning Objective : Participants will be able to: - compare and contrast the submission requirements between EU and US - devise an efficient and effective regulatory strategy for both regions
Speaker(s)
Medical Devices Regulatory Pathways across the EU and US regions
Michelle O'Connor, DrSc
ICON Clinical Research, Ireland
Director Regulatory Consulting,
Overview of Medical Device (MD) Registration and Regulations in China
Ning Li, MD, PhD
Sanofi, China
Vice President, Head of Asia Regulatory and Medical Policy
Medical Device Requirements in India
Daniel Verstappen, RN
GE Healthcare, France
Vice President Quality & Regulatory Affairs Europe - EAGM – India
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