Trial Management
  • » Feasibility studies
  • » Study design and protocol development
        (supervised by KOL expert in that field)
  • » Revision and adjustment of protocol design
        (supervised by KOL expert in that field)
  • » Sample size estimate/statistical analyses plan (SAP)
  • » Investigator selection credentialing and mapping
        of centre recruitment based on Centre
        clinical trial experiences
  • » EC submissions and Administrative/regulatory steps
  • » CRF/eCRF design for easy completion
        by the investigator and real-time analysis
  • » Patient recruitment education and retention
  • » Repackaging coding and labelling
        of investigational drug