About IDDI

We are an expert clinical data services and high-level strategic consulting contract research organization (CRO), providing agile clinical trials services for pharmaceutical, biotech, and medical device/diagnostic companies.

With a proven track record, IDDI provides expert Biostatistics and Clinical Data Science Services to ensure the successful execution of your clinical development program.

Passion. Science. Experience.

A passionate and experienced science-led team, committed to delivering submission-ready clinical data.

At IDDI our focus is on our people; our passion is advancing innovative biomedical research.

 

Meet Our Team

Commitment to Quality and Precision

“IDDI was of great benefit, particularly with respect to their responsiveness, their commitment to quality and precision, and their ability to meet our very ambitious timelines.”

Jim Taylor, CEO Oraya Therapeutics, Newark, CA, USA

32
Years in Business
1395
Phase I-IV Trials
350
Customers Worldwide
950
Scientific Publications
800
Scientific Conferences

How IDDI Adds Value to Your Clinical Data

Strategic-level consultancy to optimize your clinical development program even in clinical trials with complex settings.

Delivered by talented, forward-thinking and science-led professionals, who will take ownership of your needs.

Over 30 years in business ensuring continuity in your clinical development.

IDDI’s culture is scientifically driven, thanks to its founder and Chief Scientific Officer, Marc Buyse, ScD.

Expert clinical data services (EDC/RTSM/Medical Coding) providing flexible solutions for collection, standardization, analysis, documentation and reporting of your clinical data.

A Project Manager is assigned to every project. Flexibility, responsiveness, proactiveness are skills often mentioned by our customers.

Experienced contract research organization with a solid understanding of the clinical development process and breadth of therapeutic areas expertise.

Thanks to a strong collaborative approach with Academics and Key Opinion Leaders.

Resource Library

Discover our on-demand recorded webinars, podcasts, videos and scientific articles.

Careers

Fast growing company – Rewarding career. Join us and contribute to the progress of clinical research. An inspiring and exciting career with international and challenging projects is waiting for you!

Join Us
Featured Webinar

September 19, 2023

Good Morning Meeting | Optimizing the Transition from early to late phase trials in oncology

Subgroup Analysis in Early Drug Development

View Webinar
News & Events

IDDI hosting CDISC trainings in Raleigh, NC

April 8, 2024

Join the IDDI team for a week of in-person CDISC training from April 8 to 12.  IDDI is pleased to…

News & Events

IDDI at the 11th Annual Clinical Trials in Oncology West Coast 2024

April 23, 2024

Meet IDDI at the Clinical Trials in Oncology West Coast Annual Conference in Burlingame, CA on April 23-24! Attending CTO…

News & Events

IDDI at OCT Southeast 2024

April 16, 2024

Meet IDDI experts at OCT Southeast 2024 in Cary, NC, April 16-17! IDDI is thrilled to be in North Carolina…

News & Events

IDDI at BIO-Europe Spring 2024

March 18, 2024

Meet the IDDI team at the upcoming BIO-Europe Spring 2024 in Barcelona, Spain from March 18 to 20. Visit Booth…

News & Events

IDDI at Clinical Research Day AFCROs 2024

March 14, 2024

Meet IDDI’s Erik Falvey at this year’s Clinical Research Day by AFCROs 2024 taking place in Paris on March 14!…

News & Events

IDDI at AD/PD 2024

March 5, 2024

Meet IDDI expert at the AD/PD 2024 conference in   Are you coming to the AD/PD 2024 – International Conference on…

News & Events

IDDI exhibiting at ACDM24

March 3, 2024

Meet the IDDI experts at the upcoming ACDM24 in Copenhagen, Denmark from 3-5 March – Visit our Booth #41! Schedule…

News & Events

Understanding the EDC Set-Up Process in Clinical Trials

  In the rapidly evolving landscape of clinical research, Electronic Data Capture (EDC) systems have become indispensable. EDC systems streamline…

News & Events

Best Practices to Accelerate Your Database Lock

  Accelerating database lock in clinical research is a critical aspect of ensuring timely study conclusions and decision-making. Database lock…

News & Events

The Key to Successful Regulatory Submission: Ensuring 100% SDTM Compliance in Your SAS Database

In the complex and highly regulated world of clinical trials, the submission of data to regulatory authorities is a critical…