Our experience

  • protocols and CRFs/eCRFs: development, design and implementation
  • databases: design, development and management
  • multimedial support: project, design and implementation
  • authorisations: preparation, submission and follow-up
  • financial aspects: contracts and payments
  • selection of sites and investigators
  • clinical monitoring from pre-study to close-out visit
  • data management from CRF to statistical analysis
  • management of paper and electronic archiving
  • continuous clinical education and technical updating
  • specialised staff training (CRA, CTA, PM)
  • substantial support to medical management
  • high level medical and scientific translations
  • tracking and reconciliation of serious adverse events
  • organisation and management of investigators’ meetings
  • thorough literature search