Phase II-IIIb

ICON provides a range of integrated services that cover the planning, management, execution and analysis of Phase II – IIIb trials.

Strategic Consultancy


Our scientific and operational expertise begins with pre-clinical product planning and includes clinical development support (Phases I–III), full-service post-approval research (Phase IV and observational), and scientific and medical communications.

ICON’s Lifecycle Sciences group offers the full range of services to assist clients with activities throughout the product lifecycle.

Our comprehensive expertise is both scientific:

  • Health Economics
  • Outcomes Research
  • Epidemiology Research
  • Observational Research (including registries and safety surveillance)
  • Phase IV Research (large simple trials)
  • Statistical Analysis
  • Scientific and Medical Communications

And operational:

  • Study Start-Up
  • Site Recruitment and Site Monitoring
  • Development of Study Materials
  • Global Site Management
  • Targeted Data Management
  • Data Collection (including EDC, ePRO, and paper)
  • Statistical Programming
  • Project Management
  • Help Desk for Patients and Sites
  • Custom Technology Solutions
  • Scientific Advisory Boards