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Display Event - Drug Registration Pathways in China
Display Event - Drug Registration Pathways in China
The webinar will provide a high-level overview of the regulatory environment for medicines in China,
including regulatory authorisation pathways.
Overview
This webinar provides an overview of the regulatory requirements in China. The talk will include
registration classes of chemicals and biologics, administration fees and application timelines and
will also touch on submission dossier requirements and approval pathways.
Learning objectives
By engagement in this webinar, the delegate will:
Target audience
Regulatory professionals in UK and EU who want to familiarise themselves with the Chinese
Regulatory environment for medicines
Investors who want to understand more about key requirements for portfolio companies
Presenters
Guo Ning
Hamish King
Admitted as a lawyer in Hong Kong and in New South Wales, Australia and
formerly with Magic Circle firm Linklaters in Hong Kong, Hamish lives in Hong
Kong regularly writes and presents on China regulatory affairs life sciences
topics.
CPD
This course offers 1 CPD hour for successful completion. To learn about why CPD is important visit
the Lifelong Learning page.
How do I register?
Simply log in or create an account and register below.
Prices
Type Member Non-member
Discounted Places
A limited number of discounted places are available at the rates below for those:
Please email meetings@topra.org for a discount code before making your booking.
When 26/04/2022
Where ONLINE
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NOTE
Important instructions before booking - If your company name or VAT number does not appear here or you
would like to be invoiced using a different VAT number, please email finance@topra.org
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