International drug development Institute // Drug Repurposing

International drug development Institute

Active in Europe, the United States and Asia, a company respectfully established in the fields of biostatistics, data management and central randomization, IDDI has created a new monitoring system responding to the importance and high recommendation of central statistical monitoring (CSM) and the need for their expertise in this type of monitoring.

A pioneer in the field of central statistical monitoring, IDDI, in collaboration with Belgian entities ULB (IRIDIA), GSK Biologicals and UCL (ISBA), is developing and validating a system for monitoring and the statistical control of data quality of clinical trials, primarily based on multiple statistical tests whose results can be exploited by data mining tools and artificial intelligence designed not only to detect anomalies in data due to errors, but also negligence and fraud.

The project known as SMART (Statistical Monitoring Applied to Research Trials), developed with the financial support of the Walloon Region, aims to provide statistical monitoring with an ability to detect the heterogeneity of data throughout investigational centers and to create a quality label for clinical trial data.

While detection of deliberate (fraud) or unintentional errors is a concern at the highest level of pharmaceutical and biotechnology companies, there is currently no integrated and automated system to monitor the quality of data based on statistical tests and techniques of artificial intelligence or data mining.

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