IDDI, Biostatistical and eClinical Services for Clinical Trials

TRIAL DESIGN - RANDOMIZATION - DATA MANAGEMENT - BIOSTATISTICS
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IDDI Strengths

At IDDI, we believe that the most efficient and cost-effective way to conduct and control clinical trials is to make the best possible use of statistical methodology in their design and analysis, and of advanced web technology in their conduct supported by operational excellence. From beginning to end our constant focus is on the clinical data and we make sure they are ready for submission. 

 

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EXPERTISE IN BIOSTATISTICS 

Statistics is at the forefront of IDDI processes. Recognized as leader in the field of protocol design, biostatistics analyses, biomarkers validation and IDMC reports. Focus on the optimal design and using the clinical data that is really neededNumerous Publications

 

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INTEGRATED eCLINICAL SOLUTIONS 
Enabling cost-effective and user-friendly web systems integrating EDC, IWRS and medical coding. Faster study start-up.
 

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HIGHLY SKILLED PEOPLE
With scientific background. Bringing flexibility and ensuring continuity because of their loyalty (low turn-over <2%). Accelerated timelines in a flexible manner.
 

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THERAPEUTIC EXPERIENCE 
900+clinical trials since its inception with a focus on oncology and ophthalmology, cardiology infectious diseases, biosimilars, medical devices and more.
 

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BROAD GEOGRAPHIC REACH 

Projects across multiple continents are managed from Belgium and the US.
Academic collaborations with institutions in North America, Europe and Asia.
 

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CUSTOMER LOYALTY

Strong customer loyalty, as evidenced by a 80% repeat business rate

 

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STRONG R&D CAPABILITIES

Expertise in biostatistics leads to develop new statistical methodologies (e.g. Bayesian method for the validation of biomarkers). SMART engine (Statistical Monitoring Applied to Research Trials) which led to the foundation of CluePoints