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|About||Biostatistical and eClinical Services for phase I-IV clinical trials. Trial Design - Randomization - Data Management - Biostatistics|
|Mission||IDDI’s mission is to optimize the clinical development of drugs, biologics and devices, using a unique combination of advanced biostatistics and innovative clinical data management technology.|
IDDI (International Drug Development Institute) provides Biostatistical and eClinical Services for phase I - IV clinical trials offering trial design - randomization (IWRS) - data management - biostatistics.
IDDI combines expert methodology in Biostatistics (including Biomarkers validation and Support to IDMCs) with innovative integrated technology (eClinical suite of made-to-measure secure web systems: IWRS integrated to EDC) to optimize the design and conduct of clinical trials.
IDDI ‘experience: 16 FDA/EMA market approvals - 500+ trials to date.
IDDI is headquartered in Belgium with offices in the US (Boston, MA and Raleigh, NC)
IDDI Clinical Data Expertise leads to FDA/EMA Approval thanks to high QUALITY RISK MANAGEMENT
IDDI aims to limit risks for sponsors during the entire clinical trial process:
At the design stage: by identifying the optimal trial design
At the planning stage: by identifying key clinical data to be collected and analysed in real-time
At the conduct stage: by using web-based integrated systems to access, control and validate the data
At the analysis stage: by using advanced statistical methodology
At the report stage: by being strictly compliant to regulatory requirements
Our experts offer flexible and innovative solutions for clinical research and are not afraid to challenge the status quo.
We manage simple and complex clinical trials including adaptive trials and have all our operational systems and processes adaptive.
• The 3 Pillars of IDDI
Methodology, Technology and People, are the three 'pillars' of our highly skilled clinical research service offering: eClinical and Biostatistical services for clinical trials since 1991.
Best in class biostatistical expertise
⇒ Focus on the optimal design and using the clinical data that is really needed
Cost-effective, user-friendly integrated IWRS/EDC
⇒ Accelerated study start-up time
Highly skilled people demonstrating flexibility & continuity. Accelerated timelines in a flexib
|Founded||Marc Buyse, ScD|