Services flyers

Our experience reflects of a high value clinical trial expertise helping Sponsors to mitigate risks during the entire clinical trial process. Since 1991, we have provided quality, submission-ready data, thanks to a unique combination of methodological excellence and operational efficiency.

Overview of IDDI Clinical Trials Services

Services flyers

Clinical Trials Services: Biostatistics and integrated eClinical Solutions for Phase I-IV Clinical Trials Full range of Clinical Trials Services: Study Design – Randomization – Clinical Data Management – Biostatistics – Medical Writing IDDI is a leading, therapy-focused functional CRO combining […]

Download/View

Clinical Biostatistics Services

Services flyers

Clinical Biostatistics Services: IDDI Adds Critical Thinking to Advanced Biostatistics. Full range of clinical biostatistics services We provide advanced clinical biostatistics services for leaner and more efficient clinical trials. At IDDI, Biostatistics is at the heart of every clinical study—driving […]

Download/View

Integrated eClinical Solutions

Services flyers

Enabling Integrated eClinical solutions Single Front-End for EDC – IWRS/IRT – Drug Supply Management and Medical Coding IDDI’s eClinical services and teams take you from study initiation to database lock in the shortest possible time without compromising the accuracy and quality of your […]

Download/View

Oncology Services

Services flyers

Oncology CRO Providing Full Range of Biostatistics and eClinical Solutions IDDI is an oncology CRO led by a highly-skilled biostatistical and clinical team of thought-leaders in oncology research. 66% of our studies are in oncology. We have designed, collected, analyzed clinical […]

Download/View

Consultancy Services

Services flyers

Clinical Research Consultants Our Clinical Research Consultants provide Clinical, Statistical and Regulatory Expert Services to accelerate the development of your drug, biomarker or medical device High-level strategic services ranging from clinical study design and protocol development to regulatory submission and FDA/EMA meeting […]

Download/View