Adult clinical development takes a long time. Pediatric development takes even longer. I-ACT for Children closes this gap by connecting clinical trial sponsors and stakeholders to the pediatric experts, sites and other resources needed to conduct efficient clinical trials in children.
From protocol development to labeling, I-ACT for Children helps accelerate your pediatric clinical trials, create measurable outcomes and deliver new therapies that meet regulatory obligations and bring vital treatments to younger populations.
Our Capabilities
Strategy and Planning
- Study Feasibility & Design
- Protocol Development
- Medical & Scientific Strategy
- Real-World Data Enabled
Enable Innovation
- Pre-competitive Projects
- Platform Trials
- Advancing New Methodologies
- Communication Platforms to Share Research Practices
- Real-World Data
Trial-Ready Sites
- Training, Organization & Contract Processing
- Site Identification & Engagement
- Central IRB
- Metrics
- Pediatric Clinical Research Training
- Quality Improvement (PICTR)
Rapid Access to Network of Experts
- Scientific & Medical Experts Across Therapeutic Areas
- Timely Setup of Advisory Boards & Expert Panels