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
- Study optimization consulting utilizing proprietary PRO PASS® patient platform
- 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
