Clinical Development Group (CDG) provides expert drug development support through strategic consulting, and clinical trial oversight and operations.

Our clinical research services provide a comprehensive approach to both early and late stage drug development projects. Our clients are part of industry, academic, and research organizations. The CDG model is equally adaptive for a virtual organization or a global company.

Utilizing our drug development and regulatory expertise, primarily in oncology, we execute clinical trials efficiently and cost effectively.

CDG’s Strategic Drug Development Consulting

Our regulatory experience spans the entire drug application process from pre-IND through product approval.

• Regulatory strategy
• Protocol development
• Clinical development planning
• DSMB and SAB formation and meeting coordination
• Publication planning

CDG’s Clinical Trial Oversight and Operations

We have an extraordinary network of key investigators, and solid operational processes for site management, support and training.

• Clinical operations
• Project Management
• Clinical study team relationship management
• One-on-one investigator resource