Clinical Development Solutions Brochure

UBC’s experience in strategic clinical development and execution of both registrational and peri-approval studies includes four decades of expertise across an extensive number of therapeutic areas. UBC’s operational teams collaborate with sponsors to help ensure conclusive study results and meet global regulatory submission requirements. Our insights about patient and population dynamics, global treatment standards and practice patterns support both successful study launches and study conduct globally.

Reducing Cost with Innovation

Recognizing sponsors' multiple cost drivers, our collaborative team of project managers, CRAs, physicians, nurses, statisticians, epidemiologists, safety specialists, data managers, and medical writers will ensure conclusive study results through:

• Innovative, practical, and scientifically rigorous study designs
• Cycle-time reductions through smart feasibility assessments, streamlined start-up processes, and proactive study management
• Quality metrics for customized, flexible reporting on operational data to make the right decisions early and ensure high quality data and accelerated timelines
• Cross-functional risk-based monitoring techniques
• Technology-enabled physician and patient recruitment, resulting in accelerated enrollment and high patient retention
• Deployment of home health nurses to reduce costs