iDert is designed to meet the needs of clinical research personnel - such as data managers, biostatisticians, programmers, regulatory affairs, etc
iDert, integrated data extraction and reporting tool, is an outcome of integrating clinical and non clinical data from multiple sources into a single environment where it can be standardized, analysed, visualised and reported on by clinical researchers to regulatory agencies in shorter span of time from last observation last visit.
iDert brings a complete set of process automation using the implementation of clinical meta data repository model across different stages of clinical development by enabling the user to view, transform, analyse and report data across clinical applications, and across projects or trials within the same environment and in a regulatory compliant manner.
This is achieved in iDert by extracting data from various sources that are prevalent for a study and creating a fully controlled, traceable, complete GCP and 21 CFR Part 11 compliant data for various modules that are integrated in the product.
- involved in the integration, management, analysis and reporting of clinical trial data and align with the organisation process standards.
