Study monitoring

Our skilled and well-trained clinical research associates (CRAs) ensure the highest quality data review and effective interaction with study sites. Our CRAs conduct on-site monitoring visits throughout the study to:

  • oversee data collection and recording;
  • review source documentation and case report forms;
  • ensure regulatory compliance;
  • resolve data queries;
  • conduct interim analyses as requested by customers; and
  • set-up a data safety monitoring board (DSMB).