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Writing of Application Materials
     Review the reports of pharmaceutical, pharmacological, pharmacological and toxicological studies to meet reporting requirements
     Preparation of a complete set of IND reporting data including review of information, pharmaceutical information, pharmacology and toxicology information, clinical research data and researchers

Tracking and communication of the declaration process
     Preparation of pre-clinical communication sessions and review of the technical information needed for expert group meetings
     Follow up the whole process of reporting, professional and efficient communication with the drug trial center and the hospital, the review process smooth without delay
     To participate in the review of the expert group meeting
      Responses to the development of countermeasures and preparation questions




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