"Today, the path from initial demonstration that a molecule may have therapeutic potential to the production of an approved drug involves pre-clinical testing, complex clinical trials in humans, and post-trial regulatory approval by the FDA. For drugs, this process can take 10 to 15 years and cost millions of dollars. …

"Now, we focus on data exceptions and data analysis as opposed to data entry,?said Kathy Kerr, HR Shared Services Supervisor. ?We only work the problems.? Additionally, Kerr notes that the automation has increased the number of audits her team can run and analyze. These audits on employee data identify when …