Clinical development and regulatory services to support clients of all sizes optimize their drug development strategy and focus investments on the most promising compounds.

  • Target product profiles and clinical development planning
  • Study design and inclusion/exclusion (I/E) modeling
  • Protocol development
  • U.S. and EU regulatory strategies and management
  • Scientific advisory board management
  • Licensing opportunities
  • Medical writing
  • Presentation development and abstract submissions for medical conferences and journals