clinical monitoring

Convex CRO offers a full range of monitoring services in:


  • Phase I–IV studies on drugs
  • Bioequivalence and bioavailability studies
  • Clinical studies on food supplements
  • Clinical studies on medical devices
  • Clinical studies on vaccines


Convex monitoring team consists of full time Clinical Research Associates who guarantee up-to-date knowledge of the clinical trials’ status at each clinical site. Our monitoring procedures include:


  • Evaluation of the study 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)
  • Identification of issues and implementation of corrective actions
  • Maintenance of frequant and direct communication plan
  • Maintenance of tracking reports


Our well trained CRA team allows your project to stay in progress.  We have delivered accurate and evaluable data to our clients from over 260 successfully completed clinical studies.