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 RTSM 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 RTSM
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, RTSM and medical writing) for collection, standardization, analysis, documentation and reporting of your clinical data,
- Integrated web-based data management (EDC/RTSM/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 29 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|
January 28, 2021 | Demystifying Clinical Systems Integration
Join IDDI and XClinical for a complimentary webinar on the importance and the benefits Clinical Systems Integration JANUARY 28, 2021 - @ 11am – 12pm EST / 5pm – 6pm CET REGISTER HERE ABSTRACT: Clinical Trials have become extremely complex as well as clinical systems to an extent their integration...
February 11, 2021 | Bias and Randomization 1980 – 2020 – 2060
Learn on history of bias and randomization in oncology clinical trials and how to think about what constitutes persuasive evidence of treatment efficacy and safety February 11, 2020 - 11am-12pm EST - 5pm-6pm EST REGISTER TODAY ABSTRACT: In 1980 Jay Herson published the paper “Patient Registration in a Cooperative Oncology...