Overview
FDA Clinical Trial Data Extraction using TruAI
Pharmaceutical companies conduct Clinical Trial Analysis in a highly dynamic environment and the results have to be processed faster for further process execution. Similarly, governance bodies and regulators, like FDA, conduct separate trials to bring the product in the market after undergoing stringent evaluations.
The Clinical Trials produce machine-generated unstructured content after each lab trial. This content is stored at pre-defined shared paths or URLs belonging to the FDA, from which it needs to be extracted in a structured format and integrated with downstream systems.
This video demonstrates how TruAI uses Advanced Artificial Intelligence techniques, such as NLU, to automate data extraction and integration seamlessly in an agile environment.
