Convex’s monitoring team consists of full- and part-time Clinical Research Associates (CRAs) who guarantee up-to-date knowledge of the clinical trials’ status at each clinical site.

convex-monitoringOur monitoring procedures include:

  • Evaluation of the study’s progress
  • Review of the staff and facilities at the clinical sites
  • Review of Protocol compliance
  • Review of CRFs and performance of SDV
  • Review of Investigator’s File
  • Review of Biological Sample Handling
  • Review of Investigational Product(s)
  • Implementation of Corrective Actions
  • Addressing Administrative Issues
  • Maintaining tracking reports, etc.