Beaconcure

the integrity of clinical data, in regulatory submissions in particular, is a critical hurdle that every biopharmaceutical company must overcome to conduct clinical trials, commercialize products and maintain products in the market. the majority of all submission types carry human made errors or inconsistencies which are costing pharma, and cros valuable time and significant cost to amend. beaconcure's first application is a unique text analytics ai solution to address submission documentation quality control needs. with beaconcure, companies can quickly and effectively validate the summary data against the sources, correct inconsistencies in clinical data tables and text, and produce error-free submissions ready for regulatory approval. direct key benefits to pharma and cros: 1. accelerated turnaround: dramatically reduce months of quality control teamwork to a few days 2. eliminate inconsistences: confirm summary documentation is clean of human errors and fully backed up by the sourc