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Our experience reflects of a high value clinical trial expertise helping Sponsors to mitigate risks during the entire clinical trial process. Since 1991, we have provided quality, submission-ready data, thanks to a unique combination of methodological excellence and operational efficiency.

ID-Supply – Drug Supply Management

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Clinical Trial Drug Supply Management System. Drug Supply Management is performed via ID-supply™, it is an optional feature within our IRT system (IWRS), ID-net™.  ID-supply™ is a real time workflow management system for clinical drug supply that allows efficient drug distribution to clinical […]

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ID-Code – Medical Coding Services

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Medical Coding Services ID-code: Medical Coding System fully integrated into our EDC system. We provide medical coding services via ID-code. At IDDI medical coding is a real-time process resulting in substantial costs and time savings. AEs, SAEs and medical history are […]

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Statistical Biomarker Validation

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IDDI Accelerates Your Statistical Biomarker Validation IDDI has experience in the identification and statistical biomarker validation of diagnostic utility, prognostic and/or predictive ability, and those that can potentially be used as surrogate endpoints in clinical trials. IDDI Expertise in Statistical Biomarker Validation: We have developed a […]

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Data management for Adaptive Monitoring – KRIs

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Key Risk Indicators (KRIs): A flexible approach to adaptive monitoring in multi-center clinical trials. IDDI delivers statistical quality control of a trial based on statistical programs for the calculation of Key Risk Indicators (KRIs). Discover our services on Key Risk […]

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