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Business Development
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Clinical and regulatory
Clinical trial operation experience: Conducted dozens of clinical trials in total
Expertise in registration and regulatory affairs: by 2023, dozens of regulatory approvals have been obtained in Chinese Mainland, Hong Kong, Canada, Hungary, the United Arab Emirates, Ecuador, Mexico, Argentina, Chile, Brazil, Russia, Malaysia, Indonesia, Pakistan, Kyrgyzstan and other places
Manufacturing
The quality management system has obtained GMP certification from both China and the European Union
Compliant with international standards, including regulations and guidelines of WHO/USFDA/EU/NMPA
Commercialization
One stop vaccine supply and service
Building new speeds and capabilities to accelerate vaccine acquisition and commercial expansion
  • Innovative business models
  • Wide channel coverage
  • Efficient market access
  • High market share of listed products