Regulatory Affairs, Safety, and Clinical R&D are traditionally managed as three separate departments, each with their own business processes and software systems. Although they have functioned as silos in the past, there is an ever-growing need for sharing information within these functional areas.

As the number of these touch points increase, it motivates the desire and urgency for better integration. An analysis of how processes and systems can better integrate around these touch points can be an eye-opener for life science organizations in their quest to operate more nimbly, reduce data discrepancies, and lower costs.