The Most Intuitive EDC Suite on the Market
Featuring superior usability and flexibility, TrialMaster® is the EDC solution for Phase I – IV clinical trials
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 Anju AutoEncoder provides a modern and sophisticated tool for performing these coding activities. Out of the box it is fully integrated with Anju’s TrialMaster® product for Electronic Data Capture (EDC), but its open interfaces allow for integration with any third-party EDC or safety reporting system.
The Anju AutoEncoder is a modern and sophisticated tool for consistent and accurate coding. Out of the box, it is fully integrated with Anju’s TrialMaster® product for Electronic Data Capture (EDC), but its open interfaces allow for integration with any third-party EDC or safety reporting system.
Anju is dedicated to the process of enhancing a patient’s quality of life by reducing the time to market of essential life-saving treatments.
Pharmaceutical, biotechnology, contract research organizations, diagnostic and device firms, and academic medical centers partner with Anju to maximize the value of their clinical research investments and to develop safe and effective healthcare treatments for patients.