AutoEncoder Brochure

When conducting clinical trials or monitoring safety for approved products, the regulatory agencies require that adverse events be coded against the MedDRA dictionary, and that medications be coded against the WHODrug dictionary. The source terms are usually entered in free text, and the coding process is performed by specialist medical professionals, who must ensure consistent and accurate decisions based on the content of the source term, any relevant related data, and prior decisions for the trial or drug project.

The OmniComm AutoEncoder provides a modern and sophisticated tool for performing these coding activities. Out of the box it is fully integrated with OmniComm’s TrialMaster® product for Electronic Data Capture (EDC), but its open interfaces allow for integration with any third-party EDC or safety reporting system.