Clinical Study Design
Bringing together decades of expertise to provide optimal study design for your clinical trials, enabling you to expedite and optimize the success of your development program.
Faster study set-up using our innovative in-house interactive web response technology, dedicated to randomization and drug supply management. Integrated with EDC.
Clinical Data Management Services
Enabling end-to-end comprehensive clinical data management solutions that improve the speed and quality of your clinical trials. User-friendly, cost-effective, fully CDISC-compliant EDC. Integrated with IWRS.
Biostatistics and eClinical Services
for Clinical Trials
IDDI is 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 will help to ensure the successful execution of your clinical development program.
How IDDI Adds Value to Your Clinical Data?
- We are committed to providing quality, submission-ready clinical data, thanks to a unique combination of methodological excellence and operational efficiency:
- Strategic-level consultancy to optimize your clinical development program. Clinical study design expertise, even in your clinical trials with complex settings,
- Expert clinical data services providing advanced flexible solutions: State-of-the art methodology (biostatistics, clinical data management/EDC, IRT/IWRS and medical writing) for collection, standardization, analysis, documentation and reporting of your clinical data,
- Integrated web-based data management (EDC/IRT/medical coding) for an efficient start-up of your clinical trials,
- Delivered by an experienced stable and flexible team who will take ownership of your needs.
- We set trends in clinical research, thanks to a strong collaborative approach with Academics and Key Opinion Leaders.
- Therapy-focused CRO: Our experts are recognized worldwide.
- Over 27 years in business ensuring continuity in your clinical development.
TOP REASONS TO PARTNER WITH IDDI:
|√ Advanced Methodology||√ Clinical, Statistical & Regulatory Consultancy||√ Effective Integrated eClinical Services|
|√ Therapeutic Expertise||√ Strong R&D Capabilities||√ Flexible Service Offering|
|√ Highly Skilled Team||√ Efficient Project Timelines||√ Proven Success and Experience|
September 25, 2018 | Assessing Treatment Benefit in Immuno-Oncology
Free Live Webinar: Assessing Treatment Benefit in Immuno-Oncology Join us for a free webinar on the assessment of treatment benefit in immuno-oncology! In this webinar we will review key issues related to endpoints in immuno-oncology, with a brief overview of the four different sets of criteria for response assessment in immunotherapy....
News & Events
October 22, 2018 — October 23, 2018 | IDDI Sponsor at IRT 2018 USA
Best Practices and Innovations in IRT IDDI Sponsor and Exhibitor at CBI’s 8th Annual Interactive Response Technologies in Clinical Trials – IRT 2018! The IRT continues to gain momentum as a critical component to clinical trial and supply chain strategy, and as the complexity of trials continues to rise, creating efficiencies...
News & Events
October 19, 2018 — October 23, 2018 | Meet our Experts at ESMO 2018
LET’S MEET AT ESMO 2018! Our valuable therapeutic insight in cancer research, paired with data quality expertise, will make a critical difference to the outcome of your clinical trials. Schedule some time to meet with IDDI Oncology Experts at ESMO 2018 to discuss your situation and see how we can help...