Each clinical trial passes uncharted territory. We are your pathfinder, exploring the road ahead so you can confidently set out on the costly journey of your clinical trial.
INDEPENDENT & OBJECTIVE
CDDI is a specialist bio-medical consulting and data analytics company. We work with Pharma companies and Biotechs to ensure their development plans, protocols and Paediatric Investigation Plans are feasible. We remove barriers for optimal patient accrual. We are not a CRO, and we are not in it with the aim of winning large CRO deals further down the line.
REAL-WORLD DATA YOU ASK FOR
Our approach is hands-on and personalized. We collect detailed, real-world data on your target population. Evidence-based Feasibility is our proprietary process that delivers an Independent Data Analytics-driven simulation of accrual.
LESS HASTE, MORE SPEED
Our proprietary process, Evidence-based Feasibility, is our contribution to more sustainability in clinical research. Less waste of resource and more long-term value for all stakeholders. As what matters in the long run, is not the first patient in, but the last patient out.
The number of patients predicted by investigators typically falls by up to 90% at the start of a study.
Only to reappear as soon as the study is over.
Dr Louis Lasagna (1923-2003)
PHYSICIAN | CLINICAL PHARMACOLOGIST