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Event Details


Pharmaceutical Regulatory Affairs in China

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Who should attend?

This seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and in-market regulatory compliance in this region. You will find this seminar useful both as an introductory and or a refresher course. Previous delegates have included: Scientists and Technical staff in: Regulatory Affairs Registration Departments Medical Directors Personnel from the following areas: Analytical Research and Development Clinical Development Quality Assurance New Business Development Regulatory Authorities



This seminar will provide a detailed overview of the key areas of pharmaceutical regulatory affairs in China, Hong Kong, Macau and Taiwan and will cover:-

All important aspects of gaining and maintaining a successful Marketing Authorisation in the region

  • Drug regulatory systems
  • An overview of import and local manufacture registration
  • Clinical product development including CMC regulatory requirements
  • An interpretation of practical aspects
  • Recent developments
  • The opportunity to exchange experiences with other delegates


GBP EUR USD Standard 1499 2099 2338 Early 1299 1819 2026 Excluding VAT @ 20.00% Book by 29 Sep to get the early booking price shown above.


Leigh White

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