Clinical Data Management (CDM) is a critical phase in clinical research, which leads to generation of high-quality, reliable, and statistically sound data from clinical trials.



StatRAC team can help you with:


Study Set-Up and Planning Activities

  • Database design
  • Configure web databases
  • Create data entry forms
  • Validation controls setup


Study conduct

  • Data entry
  • Medical coding using MedDRA and WHO
  • Data validation
  • CRF / eCRF tracking and annotation dictionaries


Database lock

  • Merge randomization code to assign treatment groups
  • Flag database records as being locked
  • Deliver database (as SAS, SPSS, Text datasets)

View Data management brochure for more details