IDDI
IDDI is a global leader in regulatory statistics and clinical data science, dedicated to improving biomedical research through advanced statistical methodologies, patient-centric solutions, and agile clinical trial services. With over 30 years of experience, IDDI supports pharmaceutical, biotech, and medical device companies across various therapeutic areas, including oncology, ophthalmology, CNS, and rare diseases. The company emphasizes quality, operational efficiency, and innovation in clinical data management, biostatistics, and strategic consulting, aiming to streamline the path to market and enhance patient outcomes.
Industries
Nr. of Employees
medium (51-250)
IDDI
Products
Central statistical monitoring software
A software tool for centralized statistical monitoring that detects site-level heterogeneity and data anomalies to support trial data quality assurance.
Patient-centric statistical analysis software
Methodology and software enabling integrated analysis of multiple patient-relevant outcomes (multi-dimension comparisons) to quantify net treatment benefit.
Central statistical monitoring software
A software tool for centralized statistical monitoring that detects site-level heterogeneity and data anomalies to support trial data quality assurance.
Patient-centric statistical analysis software
Methodology and software enabling integrated analysis of multiple patient-relevant outcomes (multi-dimension comparisons) to quantify net treatment benefit.
Services
Consulting services covering trial design, regulatory statistical input, and optimization of development programs to support regulatory submissions.
Design and operational services for randomization schemes, trial supply forecasting, logistics, and RTSM integration with statistical plans.
End-to-end data management including eCRF/EDC setup, data collection, cleaning, query management, reporting, and database lock to produce submission-ready datasets.
Biostatistical analysis, interim analysis planning and execution, independent data monitoring committee support, and final statistical reporting.
Statistical monitoring of multicenter trial data to detect anomalies, heterogeneity, and support centralized quality assurance.
Consulting services covering trial design, regulatory statistical input, and optimization of development programs to support regulatory submissions.
Design and operational services for randomization schemes, trial supply forecasting, logistics, and RTSM integration with statistical plans.
End-to-end data management including eCRF/EDC setup, data collection, cleaning, query management, reporting, and database lock to produce submission-ready datasets.
Biostatistical analysis, interim analysis planning and execution, independent data monitoring committee support, and final statistical reporting.
Statistical monitoring of multicenter trial data to detect anomalies, heterogeneity, and support centralized quality assurance.
Expertise Areas
- Clinical trial design and statistical consulting
- Biostatistics and interim monitoring
- Clinical data management and EDC operations
- Randomization and trial supply management (RTSM)
Key Technologies
- Electronic data capture (EDC)
- Randomization and trial supply management (RTSM) platforms
- SDTM data standard mapping
- ADaM analysis dataset implementation
News & Updates
Visit Booth #27 to connect with clinical trials experts and explore innovative solutions to accelerate your clinical trials.
Meet with IDDI experts Jeremy Edwards and Matthew Belcher at Booth #4 to discuss how IDDI can support your clinical trials.
Join IDDI at booth #9 to learn about their clinical data services and strategic consulting.
Discover how IDDI can help with your clinical trials at Booth #29, and meet with experts like Matthew Belcher and Payton Edwards.
Meet IDDI experts Shruti Jituri and Sarah Hale at Booth #62 to discuss your upcoming drug development projects.
IDDI has recently achieved accreditation on Medidata Rave EDC, demonstrating its dedication to providing an optimal electronic data capture solution for clinical trials.
Visit Booth #27 to connect with clinical trials experts and explore innovative solutions to accelerate your clinical trials.
Meet with IDDI experts Jeremy Edwards and Matthew Belcher at Booth #4 to discuss how IDDI can support your clinical trials.
Join IDDI at booth #9 to learn about their clinical data services and strategic consulting.
Discover how IDDI can help with your clinical trials at Booth #29, and meet with experts like Matthew Belcher and Payton Edwards.
Meet IDDI experts Shruti Jituri and Sarah Hale at Booth #62 to discuss your upcoming drug development projects.
IDDI has recently achieved accreditation on Medidata Rave EDC, demonstrating its dedication to providing an optimal electronic data capture solution for clinical trials.