

Register now to learn about the recommended pathways for market access and approval needs based on practical case studies. We will provide an overview of the regulatory landscape and key considerations for setting up a trial in those countries whether you are seeking your first market approval or looking to expand your market access in the region.
Learn how to navigate product expansion and approval in China, India, and Japan with a CE mark and FDA approval when considering:
Learn how to set up a clinical study in China, India, and Japan to pursue first-time market approval with a focus on:
Bingjia Chen
Senior Business Development Manager
IQVIA MedTech, China
Kazuaki Sekiguchi, Ph.D
Senior Clinical Strategy Director
IQVIA MedTech & BioTech, Japan & Asia Pacific
Sneha Gupta
Associate Director Regulatory Affairs
IQVIA MedTech, India
Kirti Narang
Senior Clinical Project Manager
IQVIA MedTech India