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|
News & Events
March 26, 2019 — March 27, 2019 | IDDI at Outsourcing in Clinical Trials Southeast
Are you Attending Outsourcing in Clinical Trials Southeast? Join us at OCT Southeast at BOOTH 15! Let's talk about your needs and our capabilities to help you accelerate your clinical trial timelines! 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...
News & Events
March 27, 2019 — March 28, 2019 | IDDI at MassBio Annual Meeting 2019
State of Possible Conference, MassBio Annual Meeting IDDI at MassBio Annual Meeting. Join us and let’s talk about your needs and our capabilities to help you accelerate your clinical trial timelines! 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. Vicky Martin,...
February 15, 2019 | Personalized Medicine: Getting More Out of Clinical Trials
IDDI in Contract Pharma Magazine IDDI, BMS Consortium aims to establish that the GPC statistical method can complement the design, analysis and interpretation of clinical trial results; Kristin Brooks, Contract Pharma 02.15.19 [caption id="attachment_6556" align="alignright" width="206"] CLICK HERE TO READ THE ARTICLE[/caption] Results of randomized clinical trials can be somewhat limited....