Why IDDI
Trust IDDI, Your Biostatistical and Clinical Data Partner, for a Leaner Journey to Market
Expertise and knowledge: Since 1991, IDDI combines regulatory statistics, therapeutic and biostatistical expertise with deep Randomization (RTSM) and clinical data management knowledge, ensuring clinical data ready for submission.
Strategy optimization from clinical trial design to regulatory submission
Our teams of scientific specialists use advanced biostatistical analysis to ensure data quality and integrity at each milestone while preparing your clinical data for a swift and successful FDA-EMA review.
Agile Clinical Research Services From Design to Report
When you choose IDDI as your biostatistical and clinical data partner, you’re choosing excellence, reliability, and innovation.
Therapeutic & Specialty Areas
With IDDI, drug development is powered by exceptional scientific knowledge into cancer research, ophthalmology, CNS, and rare diseases combined with unmatched data quality acumen.
1,395
Phase I-IV Clinical Trials Webinars
950
Scientific Publications
4
Papers Quoted in FDA Guidance
55
Webinars
Why You Need a Clinical Data CRO
As your biostatistical and clinical data partner, IDDI ensures your data quality and streamlines processes to mitigate the risks to your clinical data at every step of the clinical trial journey.
We are here to make sure your clinical trials succeed by providing this combination of clinical development services:
- RTSM, data collection, data cleaning, and statistical analysis in line with your protocol and clinical statistical analysis plan
- Management of all data-related activities
- Direct access to clinical research consulting team
IDDI transforms clinical research challenges into triumphs, having done over 1,400 clinical trials
Together, we will unlock new possibilities for commercial success and patient outcomes.