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Understanding Regulations in China, Japan and India for Device Expansion and Clinical Operations Excellence
Join us as we explore the advantages and intricacies to setting up a clinical study in China, India, and Japan, especially for clients based in Europe and North America. 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.

Dec 8, 2021 09:00 AM in Eastern Time (US and Canada)

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