Clinical Trial Management

2017-02-21 14:29:16
As an early stage focused full service CRO, MicroConstants China works closely with our partnering clinical sites to provide the following clinical services: 
  • Screening and qualification of clinical sites 
  • Identification of lead Principal Investigator (PI) 
  • Protocol, CRF, ICF draft/review 
  • Ethic Committee document preparation 
  • Organizing Investigator training/IM 
  • Managing subject/patient recruitment 
  • Investigational drug management 
  • Trial monitoring 
  • Trial initiation, mid-phase and end of study audits 
  • Verification of CRF data 
  • Clinical sample management 
  • AE/SAE reports 
  • Data management 
  • Biostatistical analysis 
  • Clinical summary reports 
  • Document management and archiving

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