Automating Medical and Scientific Literature Monitoring for Drug Safety (PV)
Pharmacovigilance safety database systems are crucial in today’s Life Sciences world, where ensuring data quality is integral to help simplify the process of managing medical and scientific literature. Literature monitoring, an important process in drug safety vigilance, offers an end-to-end approach for literature surveillance in pharmacovigilance. Such processes bring a streamlined and compliant approach to the organization. Automating the process will bring many benefits, including efficiency and accuracy without additional risks.