Value proposition

Proven scientific and data quality excellence ensuring your clinical trial submissions

IDDI is a therapy-focused expert regulatory statistics, clinical data services and high-level strategic consulting contract research organization committed to increasing efficiency and mitigating risks throughout the drug development process.
For over 30 years, we have provided agile clinical trial services for pharmaceutical, biotechnology, and medical device/diagnostic companies to ensure their clinical data is ready for submission.

With a deep expertise in advanced biostatistics and study design, we also offer regulatory, statistical and clinical consultancy, comprehensive data management services and integrated RTSM-EDC for the successful execution of your clinical development program even with complex settings.

IDDI is Passion, Science, and Experience to ensure your data is ready for submission!

Clinical Development Strategy, Clinical Study design, Clinical Trial Consulting, Protocol Development, Generalized Pairwise Comparisons ( GPC), Biomarker/IVD Validation, Biostatistics , Biostatistical Analysis, Independent Data Monitoring Committees - IDMCs , Clinical Data Management, AdAM - SDTM, Randomization & Trial Supply Management - RTSM , Electronic data capture , IRT, EDC, Regulatory Statistics, Biometrics, and RTSM