IDDI covers the full spectrum of clinical data design, collection, management, analysis and reporting for Phase I to IV clinical trials. IDDI's services include: Trial design, Randomization (IWRS), Drug supply management, EDC, Medical coding, Data management, Biostatistics, IDMC support and Biomarker validation. IDDI's therapeutic areas of expertise include: oncology, ophthalmology, infectious diseases and cardiology. Our experience spans 23+ years, 500+ trials and 16 FDA/EMA approvals to-date.