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Clinical Trials & CRO >>> Regulatory Affairs
 
  • Consultation on strategic, regulatory, scientific and safety aspects of clinical development in China

  • IND, NDA and import license applications

  • Strategic regulatory advice and drug development plans for the Chinese market

  • Link with regulatory authorities

  • Professional preparation of medical reports, summaries, and other product information

  • Expertise in global regulatory affairs

The flow chart of application and approval procedure for clinical trials in China

(Source: http://eng.sfda.gov.cn/WS03/CL0769/61659.html)

 
 

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