Clinical Trials


Our offer

  • Expertise and management of all types of trials from Phase I to IV with medicinal products/medical devices,
    as well as of diagnostic, procedure and chart review studies

  • Experience in both sponsored and academic studies

  • Experience in a wide range of therapeutic areas

  • Consolidated network of academic investigational sites in 29 countries world-wide

What we can offer in the development and the conduction of such trials?

Through our organisation and networking we can offer a full range of services for clinical trial:


  • Feasibility study
  • Protocol and CRF/eCRF development
  • Procedures and guidelines
    preparation
  • Centres selection
  • Regulatory and EC submissions
  • Investigators meetings
  • Monitoring activities
  • Centres management
  • Data checks and cleaning
  • Safety data management
  • Medical Affairs and Safety
    Surveillance
  • Medical Review
  • Quality control
  • Statistical support to study design
  • Statistical analysis
  • Financial and administrative services
  • Overall study management
  • Essential documents management
  • Medical writing
  • Study reporting
  • Publications
  • Project management
  • Monitoring
  • Regulatory Affairs Management
  • Medical Reviewing/Farmacovigilance
  • Quality Assurance Management
  • Financial Accounting
  • Audit
  • Training
  • Centralised reading
    (Echo, Holter Coronographies)
  • Core Laboratory for centralised
  • Bio-analytical assays

Our network